DMD c.7542+13951G>C

Variant ID: X-31778126-C-G

NM_004006.2(DMD):c.7542+13951G>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Breakpoint junction features of seven DMD deletion mutations.

Human Genome Variation
Keegan, Niall P NP; Wilton, Steve D SD; Fletcher, Sue S
Publication Date: 2019

Variant appearance in text: rs6527115
PubMed Link: 31645977
Variant Present in the following documents:
  • Main text
  • 41439_2019_Article_70.pdf
View BVdb publication page