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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Mol Genet Genomic Med
Päätekijät: Foroud, Tatiana, Smith, Danielle, Jackson, Jacqueline, Verbrugge, Jennifer, Halter, Cheryl, Wetherill, Leah, Sims, Katherine, Xin, Winnie, Arnedo, Vanessa, Lasch, Shirley, Marek, Kenneth
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: John Wiley & Sons, Ltd 2015
Aiheet:
Original Articles
Linkit: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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