DMD c.2168+4944G>A

Variant ID: X-32558332-C-T

NM_004006.2(DMD):c.2168+4944G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males.

Molecular Autism
Chung, Ren-Hua RH; Ma, Deqiong D; Wang, Kai K; Hedges, Dale J DJ; Jaworski, James M JM; Gilbert, John R JR; Cuccaro, Michael L ML; Wright, Harry H HH; Abramson, Ruth K RK; Konidari, Ioanna I; Whitehead, Patrice L PL; Schellenberg, Gerard D GD; Hakonarson, Hakon H; Haines, Jonathan L JL; Pericak-Vance, Margaret A MA; Martin, Eden R ER
Publication Date: 2011-11-04

Variant appearance in text: rs721699
PubMed Link: 22050706
Variant Present in the following documents:
  • Main text
  • 2040-2392-2-18.pdf
View BVdb publication page