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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Detalles Bibliográficos
Autores principales: Foroud, Tatiana, Smith, Danielle, Jackson, Jacqueline, Verbrugge, Jennifer, Halter, Cheryl, Wetherill, Leah, Sims, Katherine, Xin, Winnie, Arnedo, Vanessa, Lasch, Shirley, Marek, Kenneth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2015
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4585448/
https://www.ncbi.nlm.nih.gov/pubmed/26436106
http://dx.doi.org/10.1002/mgg3.151

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4585448/
https://www.ncbi.nlm.nih.gov/pubmed/26436106
http://dx.doi.org/10.1002/mgg3.151

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