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Article

Cloning of the Laminin α3 Chain Gene (LAMA3) and Identification of a Homozygous Deletion in a Patient with Herlitz Junctional Epidermolysis Bullosa

1 Nov 1995

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 8586427
DOI: 10.1006/geno.1995.9877

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Related research

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Research trail→

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Cloning of the Laminin α3 Chain Gene (LAMA3) and Identification of a Homozygous Deletion in a Patient with Herlitz Junctional Epidermolysis BullosaPMID 8586427Read ↗

Novel compound heterozygous and homozygous variants of laminin subunit β3 gene underlie non-Herlitz junctional epidermolysis bullosa in two paternal half-brothers from Saudi Arabia.Semantic proximity Read ↗

Novel and recurrent mutations in the laminin-5 genes causing lethal junctional epidermolysis bullosa: molecular basis and clinical course of Herlitz diseaseSemantic proximity Read ↗

Structural analysis and mutation detection strategy for the human LAMC3 gene.Semantic proximity Read ↗

A stop-gain in the laminin, alpha 3 gene causes recessive junctional epidermolysis bullosa in Belgian Blue cattle.Semantic proximity Read ↗

Herlitz junctional epidermolysis bullosa: laminin-5 mutational profile and carrier frequency in the Italian population.Semantic proximity Read ↗

Natural history and clinical outcome of junctional epidermolysis bullosa generalized intermediate due to a LAMA3 mutation.Semantic proximity Read ↗

Laminin 332 in junctional epidermolysis bullosaSemantic proximity Read ↗

Targeted Inactivation of Murine Laminin γ2-Chain Gene Recapitulates Human Junctional Epidermolysis BullosaSemantic proximity Read ↗

Partial deletion of the <i>LAMA3</i> gene is responsible for hereditary junctional epidermolysis bullosa in the American Saddlebred HorseSemantic proximity Read ↗

cDNA sequence of the horse (Equus caballus) LAMA3 gene and characterization of two intronic SNP markers.Semantic proximity Read ↗

Laminin isoforms in development and disease.Semantic proximity Read ↗

Laminin 5 mutations in junctional epidermolysis bullosa: molecular basis of Herlitz vs. non-Herlitz phenotypes.Semantic proximity Read ↗

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