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Correction: A Homozygous PPP1R21 Splice Variant Associated with Severe Developmental Delay, Absence of Speech, and Muscle Weakness Leads to Activated Proteasome Function
| Autores principales: | , , , , , , , , , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Springer US
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10224824/ https://www.ncbi.nlm.nih.gov/pubmed/36941504 http://dx.doi.org/10.1007/s12035-023-03319-6 |
| _version_ | 1785050279494811648 |
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| author | Hentschel, Andreas Meyer, Nancy Kohlschmidt, Nicolai Groß, Claudia Sickmann, Albert Schara-Schmidt, Ulrike Förster, Fabian Töpf, Ana Christiansen, Jon Horvath, Rita Vorgerd, Matthias Thompson, Rachel Polavarapu, Kiran Lochmüller, Hanns Preusse, Corinna Hannappel, Luis Schänzer, Anne Grüneboom, Anika Gangfuß, Andrea Roos, Andreas |
| author_facet | Hentschel, Andreas Meyer, Nancy Kohlschmidt, Nicolai Groß, Claudia Sickmann, Albert Schara-Schmidt, Ulrike Förster, Fabian Töpf, Ana Christiansen, Jon Horvath, Rita Vorgerd, Matthias Thompson, Rachel Polavarapu, Kiran Lochmüller, Hanns Preusse, Corinna Hannappel, Luis Schänzer, Anne Grüneboom, Anika Gangfuß, Andrea Roos, Andreas |
| author_sort | Hentschel, Andreas |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-10224824 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2023 |
| publisher | Springer US |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-102248242023-05-29 Correction: A Homozygous PPP1R21 Splice Variant Associated with Severe Developmental Delay, Absence of Speech, and Muscle Weakness Leads to Activated Proteasome Function Hentschel, Andreas Meyer, Nancy Kohlschmidt, Nicolai Groß, Claudia Sickmann, Albert Schara-Schmidt, Ulrike Förster, Fabian Töpf, Ana Christiansen, Jon Horvath, Rita Vorgerd, Matthias Thompson, Rachel Polavarapu, Kiran Lochmüller, Hanns Preusse, Corinna Hannappel, Luis Schänzer, Anne Grüneboom, Anika Gangfuß, Andrea Roos, Andreas Mol Neurobiol Correction Springer US 2023-03-21 2023 /pmc/articles/PMC10224824/ /pubmed/36941504 http://dx.doi.org/10.1007/s12035-023-03319-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
| spellingShingle | Correction Hentschel, Andreas Meyer, Nancy Kohlschmidt, Nicolai Groß, Claudia Sickmann, Albert Schara-Schmidt, Ulrike Förster, Fabian Töpf, Ana Christiansen, Jon Horvath, Rita Vorgerd, Matthias Thompson, Rachel Polavarapu, Kiran Lochmüller, Hanns Preusse, Corinna Hannappel, Luis Schänzer, Anne Grüneboom, Anika Gangfuß, Andrea Roos, Andreas Correction: A Homozygous PPP1R21 Splice Variant Associated with Severe Developmental Delay, Absence of Speech, and Muscle Weakness Leads to Activated Proteasome Function |
| title | Correction: A Homozygous PPP1R21 Splice Variant Associated with Severe Developmental Delay, Absence of Speech, and Muscle Weakness Leads to Activated Proteasome Function |
| title_full | Correction: A Homozygous PPP1R21 Splice Variant Associated with Severe Developmental Delay, Absence of Speech, and Muscle Weakness Leads to Activated Proteasome Function |
| title_fullStr | Correction: A Homozygous PPP1R21 Splice Variant Associated with Severe Developmental Delay, Absence of Speech, and Muscle Weakness Leads to Activated Proteasome Function |
| title_full_unstemmed | Correction: A Homozygous PPP1R21 Splice Variant Associated with Severe Developmental Delay, Absence of Speech, and Muscle Weakness Leads to Activated Proteasome Function |
| title_short | Correction: A Homozygous PPP1R21 Splice Variant Associated with Severe Developmental Delay, Absence of Speech, and Muscle Weakness Leads to Activated Proteasome Function |
| title_sort | correction: a homozygous ppp1r21 splice variant associated with severe developmental delay, absence of speech, and muscle weakness leads to activated proteasome function |
| topic | Correction |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10224824/ https://www.ncbi.nlm.nih.gov/pubmed/36941504 http://dx.doi.org/10.1007/s12035-023-03319-6 |
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