Identification of a Japanese family with LRRK2 p.R1441G-related Parkinson’s disease

Leucine-rich repeat kinase 2 (LRRK2) is a causative gene of autosomal dominant familial Parkinson’s disease (PD). We screened for LRRK2 mutations in 3 frequently reported exons (31, 41, and 48) in our cohort of 871 Japanese patients with PD (430 with sporadic PD and 441 probands with familial PD). D...

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Main Authors: Hatano, Taku, Funayama, Manabu, Kubo, Shin-ichiro, Mata, Ignacio F., Oji, Yutaka, Mori, Akio, Zabetian, Cyrus P., Waldherr, Sarah M., Yoshino, Hiroyo, Oyama, Genko, Shimo, Yasushi, Fujimoto, Ken-ichi, Oshima, Hirokazu, Kunii, Yasuto, Yabe, Hirooki, Mizuno, Yoshikuni, Hattori, Nobutaka
Formato: Artigo
Idioma:Inglês
Publicado: 2014
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4171438/
https://ncbi.nlm.nih.gov/pubmed/24973808
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neurobiolaging.2014.05.025
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