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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Brief Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748314/
https://www.ncbi.nlm.nih.gov/pubmed/26900582
http://dx.doi.org/10.1002/acn3.281

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748314/
https://www.ncbi.nlm.nih.gov/pubmed/26900582
http://dx.doi.org/10.1002/acn3.281

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