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A cause for childhood ataxia

Genetic studies uncover a mutation in a widely conserved protein as the cause of a neurological disorder in two brothers.

Detalles Bibliográficos
Autor principal: Steffan, Joan S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786425/
https://www.ncbi.nlm.nih.gov/pubmed/26929993
http://dx.doi.org/10.7554/eLife.14523
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author Steffan, Joan S
author_facet Steffan, Joan S
author_sort Steffan, Joan S
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description Genetic studies uncover a mutation in a widely conserved protein as the cause of a neurological disorder in two brothers.
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spelling pubmed-47864252016-03-17 A cause for childhood ataxia Steffan, Joan S eLife Human Biology and Medicine Genetic studies uncover a mutation in a widely conserved protein as the cause of a neurological disorder in two brothers. eLife Sciences Publications, Ltd 2016-03-01 /pmc/articles/PMC4786425/ /pubmed/26929993 http://dx.doi.org/10.7554/eLife.14523 Text en © 2016, Steffan http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Human Biology and Medicine
Steffan, Joan S
A cause for childhood ataxia
title A cause for childhood ataxia
title_full A cause for childhood ataxia
title_fullStr A cause for childhood ataxia
title_full_unstemmed A cause for childhood ataxia
title_short A cause for childhood ataxia
title_sort cause for childhood ataxia
topic Human Biology and Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786425/
https://www.ncbi.nlm.nih.gov/pubmed/26929993
http://dx.doi.org/10.7554/eLife.14523
work_keys_str_mv AT steffanjoans acauseforchildhoodataxia
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