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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Mol Genet Genomic Med
मुख्य लेखकों: Foroud, Tatiana, Smith, Danielle, Jackson, Jacqueline, Verbrugge, Jennifer, Halter, Cheryl, Wetherill, Leah, Sims, Katherine, Xin, Winnie, Arnedo, Vanessa, Lasch, Shirley, Marek, Kenneth
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: John Wiley & Sons, Ltd 2015
विषय:
Original Articles
ऑनलाइन पहुंच: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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