Novel COL7A1 Mutations in Dystrophic Forms of Epidermolysis Bullosa
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
Reference20 articles.
1. Genetic basis of dominantly inherited transient bullous dermolysis of the newborn;Christiano;J Invest Dermatol,1997
2. A Strategy for identification of sequence variants in COL7A1 and a novel 2-bp deletion mutation in recessive dystrophic epidermolysis bullosa;Christiano;Hum Mutat,1997
3. Influence of the second COL7A1 mutation in determining the phenotypic severity of recessive dystrophic epidermolysis bullosa;Christiano;J Invest Dermatol,1996
4. Premature termination codons on both alleles of the type VII collagen gene (COL7A1) in three brothers with recessive dystrophic epidermolysis bullosa;Christiano;J Clin Invest,1995
5. Molecular complexity of the cutaneous basement membrane zone. Revelations from the paradigms of epidermolysis bullosa;Christiano;Exp Derm,1996
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