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#613688 - LONG QT SYNDROME 2; LQT2
LONG QT SYNDROME 1/2, DIGENIC, INCLUDED; LQT1/2, DIGENIC, INCLUDED
Cytogenetic locations: 1p36, 1p36
Gene summaries Genetic tests Medical literature
#609620 - SHORT QT SYNDROME 1; SQT1
Cytogenetic locations: Ocular
*152427 - POTASSIUM CHANNEL, VOLTAGE-GATED, SUBFAMILY H, MEMBER 2; KCNH2
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