A LRSAM1 mutation links Charcot–Marie–Tooth type 2 to Parkinson's disease

LRSAM1 mutations have been found in recessive and dominant forms of Charcot–Marie–Tooth disease. Within one generation of the original Dutch family in which the dominant LRSAM1 mutation was identified, three of the five affected family members have developed Parkinson's disease between ages 50...

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Библиографические подробности
Опубликовано в: :Ann Clin Transl Neurol
Главные авторы: Aerts, Marjolein B., Weterman, Marian A. J., Quadri, Marialuisa, Schelhaas, H. Jurgen, Bloem, Bastiaan R., Esselink, Rianne A., Baas, Frank, Bonifati, Vincenzo, van de Warrenburg, Bart P.
Формат: Artigo
Язык:Inglês
Опубликовано: John Wiley and Sons Inc. 2015
Предметы:
Brief Communication
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC4748314/
https://ncbi.nlm.nih.gov/pubmed/26900582
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.281
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