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Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974105/ https://www.ncbi.nlm.nih.gov/pubmed/27486784 http://dx.doi.org/10.1016/j.ajhg.2016.07.015 |
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author | Tuschl, Karin Clayton, Peter T. Gospe, Sidney M. Gulab, Shamshad Ibrahim, Shahnaz Singhi, Pratibha Aulakh, Roosy Ribeiro, Reinaldo T. Barsottini, Orlando G. Zaki, Maha S. Del Rosario, Maria Luz Dyack, Sarah Price, Victoria Rideout, Andrea Gordon, Kevin Wevers, Ron A. Chong, W.K. ‘‘Kling’’ Mills, Philippa B. |
author_facet | Tuschl, Karin Clayton, Peter T. Gospe, Sidney M. Gulab, Shamshad Ibrahim, Shahnaz Singhi, Pratibha Aulakh, Roosy Ribeiro, Reinaldo T. Barsottini, Orlando G. Zaki, Maha S. Del Rosario, Maria Luz Dyack, Sarah Price, Victoria Rideout, Andrea Gordon, Kevin Wevers, Ron A. Chong, W.K. ‘‘Kling’’ Mills, Philippa B. |
author_sort | Tuschl, Karin |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-4974105 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-49741052016-08-11 Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man Tuschl, Karin Clayton, Peter T. Gospe, Sidney M. Gulab, Shamshad Ibrahim, Shahnaz Singhi, Pratibha Aulakh, Roosy Ribeiro, Reinaldo T. Barsottini, Orlando G. Zaki, Maha S. Del Rosario, Maria Luz Dyack, Sarah Price, Victoria Rideout, Andrea Gordon, Kevin Wevers, Ron A. Chong, W.K. ‘‘Kling’’ Mills, Philippa B. Am J Hum Genet Correction Elsevier 2016-08-04 2016-08-02 /pmc/articles/PMC4974105/ /pubmed/27486784 http://dx.doi.org/10.1016/j.ajhg.2016.07.015 Text en © 2016 American Society of Human Genetics. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Correction Tuschl, Karin Clayton, Peter T. Gospe, Sidney M. Gulab, Shamshad Ibrahim, Shahnaz Singhi, Pratibha Aulakh, Roosy Ribeiro, Reinaldo T. Barsottini, Orlando G. Zaki, Maha S. Del Rosario, Maria Luz Dyack, Sarah Price, Victoria Rideout, Andrea Gordon, Kevin Wevers, Ron A. Chong, W.K. ‘‘Kling’’ Mills, Philippa B. Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man |
title | Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man |
title_full | Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man |
title_fullStr | Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man |
title_full_unstemmed | Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man |
title_short | Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man |
title_sort | syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused by mutations in slc30a10, a manganese transporter in man |
topic | Correction |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974105/ https://www.ncbi.nlm.nih.gov/pubmed/27486784 http://dx.doi.org/10.1016/j.ajhg.2016.07.015 |
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