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KCNJ5

potassium inwardly rectifying channel subfamily J member 5

gene with protein productOMIM: 6007344 заболевания

Ассоциированные заболевания

Герминативная мутация (причина)2
Disease-causing germline mutation(s) (gain of function) in1
Disease-causing germline mutation(s) (loss of function) in1