Jervell-Lange Nielsen Syndrome
"Jervell-Lange Nielsen Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
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A form of long QT syndrome that is associated with congenital deafness. It is characterized by abnormal cardioelectrophysiology involving the VOLTAGE-GATED POTASSIUM CHANNEL. It results from mutation of KCNQ1 gene (Subtype 1 or JLN1) or the KCNE1 gene (Subtype 2 or JLN2).
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