201 top medical experts on Jervell-Lange Nielsen Syndrome across 27 countries and 4 U.S. states, including 30 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- 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).
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Broader Categories (#Experts): Long QT Syndrome (3,094).
- Clinical Trials : at least 1 including 1 Completed
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