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Article

Mutations in Alport syndrome associated with diffuse esophageal leiomyomatosis.

Contributions to nephrology - 1 Jan 1996

Antignac C, Heidet L

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Share to Nephritis, Hereditary
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 8801045
DOI: 10.1159/000424813

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Mutations in Alport syndrome associated with diffuse esophageal leiomyomatosis.PMID 8801045Read ↗

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Alport syndrome and leiomyomatosis: the first deletion extending beyond COL4A6 intron 2Semantic proximity Read ↗

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Rare missense variants in the ALPK1 gene may predispose to periodic fever, aphthous stomatitis, pharyngitis and adenitis (PFAPA) syndromeSemantic proximity Read ↗

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Novel COL4A5/COL4A6 deletions and further characterization of the diffuse leiomyomatosis-Alport syndrome (DL-AS) locus define the DL critical regionSemantic proximity Read ↗

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