DMD c.8217+5G>A

Variant ID: X-31645785-C-T

NM_004006.2(DMD):c.8217+5G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Dystrophin gene mutation location and the risk of cognitive impairment in Duchenne muscular dystrophy.

Plos One
Taylor, Peter J PJ; Betts, Grant A GA; Maroulis, Sarah S; Gilissen, Christian C; Pedersen, Robyn L RL; Mowat, David R DR; Johnston, Heather M HM; Buckley, Michael F MF
Publication Date: 2010-01-20

Variant appearance in text: DMD: 8217+5G>A
PubMed Link: 20098710
Variant Present in the following documents:
  • Main text
View BVdb publication page