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Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
| Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Nature Publishing Group UK
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497626/ https://www.ncbi.nlm.nih.gov/pubmed/31048695 http://dx.doi.org/10.1038/s41467-019-10161-9 |
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| author | Snijders Blok, Lot Rousseau, Justine Twist, Joanna Ehresmann, Sophie Takaku, Motoki Venselaar, Hanka Rodan, Lance H. Nowak, Catherine B. Douglas, Jessica Swoboda, Kathryn J. Steeves, Marcie A. Sahai, Inderneel Stumpel, Connie T. R. M. Stegmann, Alexander P. A. Wheeler, Patricia Willing, Marcia Fiala, Elise Kochhar, Aaina Gibson, William T. Cohen, Ana S. A. Agbahovbe, Ruky Innes, A. Micheil Au, P. Y. Billie Rankin, Julia Anderson, Ilse J. Skinner, Steven A. Louie, Raymond J. Warren, Hannah E. Afenjar, Alexandra Keren, Boris Nava, Caroline Buratti, Julien Isapof, Arnaud Rodriguez, Diana Lewandowski, Raymond Propst, Jennifer van Essen, Ton Choi, Murim Lee, Sangmoon Chae, Jong H. Price, Susan Schnur, Rhonda E. Douglas, Ganka Wentzensen, Ingrid M. Zweier, Christiane Reis, André Bialer, Martin G. Moore, Christine Koopmans, Marije Brilstra, Eva H. Monroe, Glen R. van Gassen, Koen L. I. van Binsbergen, Ellen Newbury-Ecob, Ruth Bownass, Lucy Bader, Ingrid Mayr, Johannes A. Wortmann, Saskia B. Jakielski, Kathy J. Strand, Edythe A. Kloth, Katja Bierhals, Tatjana Roberts, John D. Petrovich, Robert M. Machida, Shinichi Kurumizaka, Hitoshi Lelieveld, Stefan Pfundt, Rolph Jansen, Sandra Deriziotis, Pelagia Faivre, Laurence Thevenon, Julien Assoum, Mirna Shriberg, Lawrence Kleefstra, Tjitske Brunner, Han G. Wade, Paul A. Fisher, Simon E. Campeau, Philippe M. |
| author_facet | Snijders Blok, Lot Rousseau, Justine Twist, Joanna Ehresmann, Sophie Takaku, Motoki Venselaar, Hanka Rodan, Lance H. Nowak, Catherine B. Douglas, Jessica Swoboda, Kathryn J. Steeves, Marcie A. Sahai, Inderneel Stumpel, Connie T. R. M. Stegmann, Alexander P. A. Wheeler, Patricia Willing, Marcia Fiala, Elise Kochhar, Aaina Gibson, William T. Cohen, Ana S. A. Agbahovbe, Ruky Innes, A. Micheil Au, P. Y. Billie Rankin, Julia Anderson, Ilse J. Skinner, Steven A. Louie, Raymond J. Warren, Hannah E. Afenjar, Alexandra Keren, Boris Nava, Caroline Buratti, Julien Isapof, Arnaud Rodriguez, Diana Lewandowski, Raymond Propst, Jennifer van Essen, Ton Choi, Murim Lee, Sangmoon Chae, Jong H. Price, Susan Schnur, Rhonda E. Douglas, Ganka Wentzensen, Ingrid M. Zweier, Christiane Reis, André Bialer, Martin G. Moore, Christine Koopmans, Marije Brilstra, Eva H. Monroe, Glen R. van Gassen, Koen L. I. van Binsbergen, Ellen Newbury-Ecob, Ruth Bownass, Lucy Bader, Ingrid Mayr, Johannes A. Wortmann, Saskia B. Jakielski, Kathy J. Strand, Edythe A. Kloth, Katja Bierhals, Tatjana Roberts, John D. Petrovich, Robert M. Machida, Shinichi Kurumizaka, Hitoshi Lelieveld, Stefan Pfundt, Rolph Jansen, Sandra Deriziotis, Pelagia Faivre, Laurence Thevenon, Julien Assoum, Mirna Shriberg, Lawrence Kleefstra, Tjitske Brunner, Han G. Wade, Paul A. Fisher, Simon E. Campeau, Philippe M. |
| author_sort | Snijders Blok, Lot |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-6497626 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2019 |
| publisher | Nature Publishing Group UK |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-64976262019-05-06 Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language Snijders Blok, Lot Rousseau, Justine Twist, Joanna Ehresmann, Sophie Takaku, Motoki Venselaar, Hanka Rodan, Lance H. Nowak, Catherine B. Douglas, Jessica Swoboda, Kathryn J. Steeves, Marcie A. Sahai, Inderneel Stumpel, Connie T. R. M. Stegmann, Alexander P. A. Wheeler, Patricia Willing, Marcia Fiala, Elise Kochhar, Aaina Gibson, William T. Cohen, Ana S. A. Agbahovbe, Ruky Innes, A. Micheil Au, P. Y. Billie Rankin, Julia Anderson, Ilse J. Skinner, Steven A. Louie, Raymond J. Warren, Hannah E. Afenjar, Alexandra Keren, Boris Nava, Caroline Buratti, Julien Isapof, Arnaud Rodriguez, Diana Lewandowski, Raymond Propst, Jennifer van Essen, Ton Choi, Murim Lee, Sangmoon Chae, Jong H. Price, Susan Schnur, Rhonda E. Douglas, Ganka Wentzensen, Ingrid M. Zweier, Christiane Reis, André Bialer, Martin G. Moore, Christine Koopmans, Marije Brilstra, Eva H. Monroe, Glen R. van Gassen, Koen L. I. van Binsbergen, Ellen Newbury-Ecob, Ruth Bownass, Lucy Bader, Ingrid Mayr, Johannes A. Wortmann, Saskia B. Jakielski, Kathy J. Strand, Edythe A. Kloth, Katja Bierhals, Tatjana Roberts, John D. Petrovich, Robert M. Machida, Shinichi Kurumizaka, Hitoshi Lelieveld, Stefan Pfundt, Rolph Jansen, Sandra Deriziotis, Pelagia Faivre, Laurence Thevenon, Julien Assoum, Mirna Shriberg, Lawrence Kleefstra, Tjitske Brunner, Han G. Wade, Paul A. Fisher, Simon E. Campeau, Philippe M. Nat Commun Author Correction Nature Publishing Group UK 2019-05-02 /pmc/articles/PMC6497626/ /pubmed/31048695 http://dx.doi.org/10.1038/s41467-019-10161-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
| spellingShingle | Author Correction Snijders Blok, Lot Rousseau, Justine Twist, Joanna Ehresmann, Sophie Takaku, Motoki Venselaar, Hanka Rodan, Lance H. Nowak, Catherine B. Douglas, Jessica Swoboda, Kathryn J. Steeves, Marcie A. Sahai, Inderneel Stumpel, Connie T. R. M. Stegmann, Alexander P. A. Wheeler, Patricia Willing, Marcia Fiala, Elise Kochhar, Aaina Gibson, William T. Cohen, Ana S. A. Agbahovbe, Ruky Innes, A. Micheil Au, P. Y. Billie Rankin, Julia Anderson, Ilse J. Skinner, Steven A. Louie, Raymond J. Warren, Hannah E. Afenjar, Alexandra Keren, Boris Nava, Caroline Buratti, Julien Isapof, Arnaud Rodriguez, Diana Lewandowski, Raymond Propst, Jennifer van Essen, Ton Choi, Murim Lee, Sangmoon Chae, Jong H. Price, Susan Schnur, Rhonda E. Douglas, Ganka Wentzensen, Ingrid M. Zweier, Christiane Reis, André Bialer, Martin G. Moore, Christine Koopmans, Marije Brilstra, Eva H. Monroe, Glen R. van Gassen, Koen L. I. van Binsbergen, Ellen Newbury-Ecob, Ruth Bownass, Lucy Bader, Ingrid Mayr, Johannes A. Wortmann, Saskia B. Jakielski, Kathy J. Strand, Edythe A. Kloth, Katja Bierhals, Tatjana Roberts, John D. Petrovich, Robert M. Machida, Shinichi Kurumizaka, Hitoshi Lelieveld, Stefan Pfundt, Rolph Jansen, Sandra Deriziotis, Pelagia Faivre, Laurence Thevenon, Julien Assoum, Mirna Shriberg, Lawrence Kleefstra, Tjitske Brunner, Han G. Wade, Paul A. Fisher, Simon E. Campeau, Philippe M. Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language |
| title | Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language |
| title_full | Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language |
| title_fullStr | Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language |
| title_full_unstemmed | Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language |
| title_short | Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language |
| title_sort | author correction: chd3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language |
| topic | Author Correction |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497626/ https://www.ncbi.nlm.nih.gov/pubmed/31048695 http://dx.doi.org/10.1038/s41467-019-10161-9 |
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