NSF c.1908+9832G>T

Variant ID: 17-44816132-G-T

NM_006178.3(NSF):c.1908+9832G>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.

Bmc Medical Genetics
Liu, Xinmin X; Cheng, Rong R; Verbitsky, Miguel M; Kisselev, Sergey S; Browne, Andrew A; Mejia-Sanatana, Helen H; Louis, Elan D ED; Cote, Lucien J LJ; Andrews, Howard H; Waters, Cheryl C; Ford, Blair B; Frucht, Steven S; Fahn, Stanley S; Marder, Karen K; Clark, Lorraine N LN; Lee, Joseph H JH
Publication Date: 2011-08-03

Variant appearance in text: rs12325819
PubMed Link: 21812969
Variant Present in the following documents:
  • Main text
  • 1471-2350-12-104.pdf
View BVdb publication page