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SPG7 mutations are a common cause of undiagnosed ataxia
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4371411/ https://www.ncbi.nlm.nih.gov/pubmed/25681447 http://dx.doi.org/10.1212/WNL.0000000000001369 |
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author | Pfeffer, Gerald Pyle, Angela Griffin, Helen Miller, Jack Wilson, Valerie Turnbull, Lisa Fawcett, Katherine Sims, David Eglon, Gail Hadjivassiliou, Marios Horvath, Rita Németh, Andrea Chinnery, Patrick F. |
author_facet | Pfeffer, Gerald Pyle, Angela Griffin, Helen Miller, Jack Wilson, Valerie Turnbull, Lisa Fawcett, Katherine Sims, David Eglon, Gail Hadjivassiliou, Marios Horvath, Rita Németh, Andrea Chinnery, Patrick F. |
author_sort | Pfeffer, Gerald |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-4371411 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-43714112015-04-06 SPG7 mutations are a common cause of undiagnosed ataxia Pfeffer, Gerald Pyle, Angela Griffin, Helen Miller, Jack Wilson, Valerie Turnbull, Lisa Fawcett, Katherine Sims, David Eglon, Gail Hadjivassiliou, Marios Horvath, Rita Németh, Andrea Chinnery, Patrick F. Neurology Clinical/Scientific Notes Lippincott Williams & Wilkins 2015-03-17 /pmc/articles/PMC4371411/ /pubmed/25681447 http://dx.doi.org/10.1212/WNL.0000000000001369 Text en © 2015 American Academy of Neurology This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical/Scientific Notes Pfeffer, Gerald Pyle, Angela Griffin, Helen Miller, Jack Wilson, Valerie Turnbull, Lisa Fawcett, Katherine Sims, David Eglon, Gail Hadjivassiliou, Marios Horvath, Rita Németh, Andrea Chinnery, Patrick F. SPG7 mutations are a common cause of undiagnosed ataxia |
title | SPG7 mutations are a common cause of undiagnosed ataxia |
title_full | SPG7 mutations are a common cause of undiagnosed ataxia |
title_fullStr | SPG7 mutations are a common cause of undiagnosed ataxia |
title_full_unstemmed | SPG7 mutations are a common cause of undiagnosed ataxia |
title_short | SPG7 mutations are a common cause of undiagnosed ataxia |
title_sort | spg7 mutations are a common cause of undiagnosed ataxia |
topic | Clinical/Scientific Notes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4371411/ https://www.ncbi.nlm.nih.gov/pubmed/25681447 http://dx.doi.org/10.1212/WNL.0000000000001369 |
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