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Article

Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome

1 Sept 1998

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9799083
DOI: 10.1007/s004390050819

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Related research

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Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndromePMID 9799083Read ↗

Large-scale mutational analysis of Kv11.1 reveals molecular insights into type 2 long QT syndromeSemantic proximity Read ↗

Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.Semantic proximity Read ↗

Molecular genetics of inherited long QT syndromes.Semantic proximity Read ↗

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangementsSemantic proximity Read ↗

Molecular genetics of long QT syndromeSemantic proximity Read ↗

Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome.Semantic proximity Read ↗

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndromeSemantic proximity Read ↗

New mutations in the KVLQT1 potassium channel that cause long-QT syndrome.Semantic proximity Read ↗

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.Semantic proximity Read ↗

Molecular basis of congenital and acquired long QT syndromes.Semantic proximity Read ↗

Integrative analysis of KCNQ1 variants reveals molecular mechanisms of type 1 long QT syndrome pathogenesisSemantic proximity Read ↗

KVLQT1 mutations in three families with familial or sporadic long QT syndrome.Semantic proximity Read ↗

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