DMD c.10546G>T ;(p.E3516*)

Variant ID: X-31187567-C-A

NM_004006.2(DMD):c.10546G>T;(p.E3516*)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A retrospective analysis of 237 Chinese families with Duchenne muscular dystrophy history and strategies of prenatal diagnosis.

Journal Of Clinical Laboratory Analysis
Xu, Ying Y; Li, Yu Y; Song, Tingting T; Guo, Fenfen F; Zheng, Jiao J; Xu, Hui H; Yan, Feng F; Cheng, Lu L; Li, Chunyan C; Chen, Biliang B; Zhang, Jianfang J
Publication Date: 2018-09

Variant appearance in text: DMD: 10546G>T; Glu3516X
PubMed Link: 29604111
Variant Present in the following documents:
  • Main text
View BVdb publication page