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Jervell-Lange Nielsen Syndrome: 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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