Linkage of Autosomal Dominant Dystrophic Epidermolysis Bullosa in Three British Families to the Marker D3S2 Close to the COL7A1 Locus.

Journal of Medical Genetics- United Kingdom

doi 10.1136/jmg.29.6.381

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June 1, 1992

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BMJ

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Amanote Research

Linkage of Autosomal Dominant Dystrophic Epidermolysis Bullosa in Three British Families to the Marker D3S2 Close to the COL7A1 Locus.

Journal of Medical Genetics- United Kingdom

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

Genetic Linkage of Type VII Collagen (COL7A1) to Dominant Dystrophic Epidermolysis Bullosa in Families With Abnormal Anchoring Fibrils.

A Case of Dominant Dystrophic Epidermolysis Bullosa Responding Well to an Old Medication

Case Report: Whole Exome Sequencing Reveals a Novel Frameshift Deletion Mutation p.G2254fs in COL7A1 Associated With Autosomal Recessive Dystrophic Epidermolysis Bullosa

Dystrophic Epidermolysis Bullosa: COL7A1 Mutation Landscape in a Multi-Ethnic Cohort of 152 Extended Families With High Degree of Customary Consanguineous Marriages

Recessive Dystrophic Epidermolysis Bullosa Inversa

Dilated Cardiomyopathy in Dystrophic Epidermolysis Bullosa

Exclusion of Linkage Between the Collagenase Gene and Generalized Recessive Dystrophic Epidermolysis Bullosa Phenotype.

Gene-Corrected Fibroblast Therapy for Recessive Dystrophic Epidermolysis Bullosa Using a Self-Inactivating COL7A1 Retroviral Vector

271 From Clinical to Genotypic Modeling: Recessive Dystrophic Epidermolysis Bullosa (RDEB)