Clinical Expression of LRRK2 G2019S Mutations in the Elderly

Mutations in the leucine-rich repeat kinase 2 gene (LRRK2, PARK8) are the most commonly identified monogenic etiology of Parkinson disease (PD). Over-represented in the Ashkenazi Jewish (AJ) population, these mutations are transmitted in an autosomal dominant manner with age-dependent reduced penetr...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Luciano, Marta San, Lipton, Richard B., Wang, Cuiling, Katz, Mindy, Zimmerman, Molly E., Sanders, Amy E., Ozelius, Laurie J., Bressman, Susan B., Saunders-Pullman, Rachel
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2010
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2978804/
https://ncbi.nlm.nih.gov/pubmed/20721910
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mds.23330
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