DMD c.4859A>G ;(p.E1620G)

Variant ID: X-32383303-T-C

NM_004006.2(DMD):c.4859A>G;(p.E1620G)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Myocardial ultrastructure can augment genetic testing for sporadic dilated cardiomyopathy with initial heart failure.

Esc Heart Failure
Saito, Tsunenori T; Sato, Naoko Saito NS; Mozawa, Kosuke K; Adachi, Akiko A; Sasaki, Yoshihiro Y; Nakamura, Kotoka K; Oka, Eiichiro E; Otsuka, Toshiaki T; Kodani, Eitaro E; Asai, Kuniya K; Mizuno, Kyoichi K; Shimizu, Wataru W; Gottlieb, Roberta A RA
Publication Date: 2021-09-06

Variant appearance in text: DMD: 4859A>G; E1620G
PubMed Link: 34486814
Variant Present in the following documents:
  • Main text
  • EHF2-8-5178.pdf
View BVdb publication page



Myocardial ultrastructure can augment genetic testing for sporadic dilated cardiomyopathy with initial heart failure.

Esc Heart Failure
Saito, Tsunenori T; Sato, Naoko Saito NS; Mozawa, Kosuke K; Adachi, Akiko A; Sasaki, Yoshihiro Y; Nakamura, Kotoka K; Oka, Eiichiro E; Otsuka, Toshiaki T; Kodani, Eitaro E; Asai, Kuniya K; Mizuno, Kyoichi K; Shimizu, Wataru W; Gottlieb, Roberta A RA
Publication Date: 2021-12

Variant appearance in text: DMD: 4859A>G; E1620G
PubMed Link: 34486814
Variant Present in the following documents:
  • Main text
  • EHF2-8-5178.pdf
View BVdb publication page