A case of long QT syndrome with triple gene abnormalities: digenic mutations in KCNH2 and SCN5A and gene variant in KCNE1 (Q85650522)
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scientific article published on 11 December 2012
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English | A case of long QT syndrome with triple gene abnormalities: digenic mutations in KCNH2 and SCN5A and gene variant in KCNE1 |
scientific article published on 11 December 2012 |
Statements
A case of long QT syndrome with triple gene abnormalities: digenic mutations in KCNH2 and SCN5A and gene variant in KCNE1 (English)
Yukako Yoshikane
Masao Yoshinaga
Kunihiro Hamamoto
11 December 2012