Scientists discover KCNH2 gene mutation in patients with long QT syndrome
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Scientists discover KCNH2 gene mutation in patients with long QT syndrome
Researchers from the Hospital Virgen de las Nieves of the University of Granada have identified the most frequent mutations in the gene KCNH2 in patients with long QT syndrome.
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Tags: Arrhythmia, Long QT Syndrome, Seizure, Epilepsy, Genes, Scientist, News, Science
Most Recently Shared on February 10, 2011 at 7:14 am By:
Epilepsy News: Scientists discover KCNH2 gene mutation in patients with long QT syndrome: Researchers from the H... http://bit.ly/hZ2Cbj
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