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Mutations in up to 15 genes have been associated with long QT syndrome (LQTS), most encoding for subunits of cardiac ionic channels. In majority of cases, each family has its… Click to show full abstract
Mutations in up to 15 genes have been associated with long QT syndrome (LQTS), most encoding for subunits of cardiac ionic channels. In majority of cases, each family has its “own” mutation. Individuals with suspected LQTS are regularly investigated in University Hospital Brno, all of them
Keywords:
073 16776;
long syndrome;
unexpectedly high;
high incidence;
16776 unexpectedly;
mutation
Journal Title: JACC: Clinical Electrophysiology
Year Published: 2017
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Journal Title: JACC: Clinical Electrophysiology
Year Published: 2017
Link to full text (if available)
Share on Social Media: Sign Up to like & get
recommendations!