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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Detalhes bibliográficos
Publicado no:Ann Clin Transl Neurol
Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2015
Assuntos:
Brief Communication
Acesso em linha: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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