HFE c.236T>A ;(p.I79N)

Variant ID: 6-26091228-T-A

NM_000410.3(HFE):c.236T>A;(p.I79N)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Complex roads from genotype to phenotype in dilated cardiomyopathy: scientific update from the Working Group of Myocardial Function of the European Society of Cardiology.

Cardiovascular Research
Bondue, Antoine A; Arbustini, Eloisa E; Bianco, Anna A; Ciccarelli, Michele M; Dawson, Dana D; De Rosa, Matteo M; Hamdani, Nazha N; Hilfiker-Kleiner, Denise D; Meder, Benjamin B; Leite-Moreira, Adelino F AF; Thum, Thomas T; Tocchetti, Carlo G CG; Varricchi, Gilda G; Van der Velden, Jolanda J; Walsh, Roddy R; Heymans, Stephane S
Publication Date: 2018-08-01

Variant appearance in text: HFE: I79N
PubMed Link: 29800419
Variant Present in the following documents:
  • Main text
View BVdb publication page



Therapeutic Strategies Targeting Inherited Cardiomyopathies.

Current Heart Failure Reports
Varian, Kenneth K; Tang, W H Wilson WHW
Publication Date: 2017-08

Variant appearance in text: HFE: I79N
PubMed Link: 28660543
Variant Present in the following documents:
  • Main text
View BVdb publication page