PAK5 c.-11-11309A>G

Variant ID: 20-9636296-T-C

NM_177990.2(PAK5):c.-11-11309A>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A genomic pathway approach to a complex disease: axon guidance and Parkinson disease.

Plos Genetics
Lesnick, Timothy G TG; Papapetropoulos, Spiridon S; Mash, Deborah C DC; Ffrench-Mullen, Jarlath J; Shehadeh, Lina L; de Andrade, Mariza M; Henley, John R JR; Rocca, Walter A WA; Ahlskog, J Eric JE; Maraganore, Demetrius M DM
Publication Date: 2007-06

Variant appearance in text: rs6086976
PubMed Link: 17571925
Variant Present in the following documents:
  • pgen.0030098.pdf
View BVdb publication page