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Article

A family of hereditary long QT syndrome caused by Q738X HERG mutation.

International journal of cardiology - 24 Sept 2010

Yasuda Shioto, Hiramatsu Shin-Ichi, Odashiro Keita, Maruyama Toru, Tsuji Keiko, Horie Minoru

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 19157587
DOI: 10.1016/j.ijcard.2008.12.053

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A family of hereditary long QT syndrome caused by Q738X HERG mutation.PMID 19157587Read ↗

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Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndrome.Semantic proximity Read ↗

A missense mutation (G604S) in the S5/pore region of HERG causes long QT syndrome in a Chinese family with a high incidence of sudden unexpected death.Semantic proximity Read ↗

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