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...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Glavni autori: 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
Format: Artigo
Jezik:Inglês
Izdano: 2010
Teme:
Article
Online pristup: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
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!

Similar Items