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Article

KCNE1-like Gene Is Deleted in AMME Contiguous Gene Syndrome: Identification and Characterization of the Human and Mouse Homologs

1 Sept 1999

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 10493825
DOI: 10.1006/geno.1999.5904

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Related research

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KCNE1-like Gene Is Deleted in AMME Contiguous Gene Syndrome: Identification and Characterization of the Human and Mouse HomologsPMID 10493825Read ↗

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An essential gene mutagenesis screen across the highly conserved piebald deletion region of mouse chromosome 14.Semantic proximity Read ↗

Loss of ERG function causes lymphatic vessel malformations and primary lymphoedemaSemantic proximity Read ↗

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Expanding the spectrum of phenotypes for MPDZ: Report of four unrelated families and review of the literature.Semantic proximity Read ↗

EGR2 mutation enhances phenotype spectrum of Dejerine-Sottas syndrome.Semantic proximity Read ↗

Expression of multiple KCNE genes in human heart may enable variable modulation ofSemantic proximity Read ↗

DFNA2/KCNQ4 and its manifestations.Semantic proximity Read ↗

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