Novel recruitment strategy to enrich for LRRK2 mutation carriers

The LRRK2 G2019S mutation is found at higher frequency among Parkinson disease (PD) patients of Ashkenazi Jewish (AJ) ancestry. This study was designed to test whether an internet-based approach could be an effective approach to screen and identify mutation carriers. Individuals with and without PD...

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Detalhes bibliográficos
Publicado no:Mol Genet Genomic Med
Main Authors: Foroud, Tatiana, Smith, Danielle, Jackson, Jacqueline, Verbrugge, Jennifer, Halter, Cheryl, Wetherill, Leah, Sims, Katherine, Xin, Winnie, Arnedo, Vanessa, Lasch, Shirley, Marek, Kenneth
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley & Sons, Ltd 2015
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4585448/
https://ncbi.nlm.nih.gov/pubmed/26436106
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.151
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