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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Vydáno v:Ann Clin Transl Neurol
Hlavní autoři: 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.
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2015
Témata:
Brief Communication
On-line přístup: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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