The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor

Background: Mutations in the gene Leucine-Rich Repeat Kinase 2 (LRRK2) were recently identified as the cause of PARK8 linked autosomal dominant Parkinson's disease. Objective: To study recurrent LRRK2 mutations in a large sample of patients from Italy, including early (<50 years) and late on...

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Главные авторы: Goldwurm, S, Fonzo, A, Simons, E, Rohe, C, Zini, M, Canesi, M, Tesei, S, Zecchinelli, A, Antonini, A, Mariani, C, Meucci, N, Sacilotto, G, Sironi, F, Salani, G, Ferreira, J, Chien, H, Fabrizio, E, Vanacore, N, Libera, A, Stocchi, F, Diroma, C, Lamberti, P, Sampaio, C, Meco, G, Barbosa, E, Bertoli-Avella, A, Breedveld, G, Oostra, B, Pezzoli, G, Bonifati, V
Формат: Artigo
Язык:Inglês
Опубликовано: BMJ Group 2005
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Electronic Letter
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC1735940/
https://ncbi.nlm.nih.gov/pubmed/16272257
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2005.035568
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