Symposium on Epidermolysis Bullosa: Molecular Biology and Pathology of the Cutaneous Basement Membrane Zone
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
Reference32 articles.
1. Revised clinical and laboratory criteria for subtypes in inherited epidermolysis bullosa. A consensus report by the subcommittee on Diagnosis and Classification of the National Epidermolysis Bullosa Registry;Fine;J Am Acad Dermatol,1991
2. Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: genetic and functional analyses;Coulombe;Cell,1991
3. Mutant keratin expression in transgenic mice causes marked abnormalities resembling a human genetic skin disease;Vassar;Cell,1991
4. Epidermolysis bullosa simplex: evidence in two families for keratin gene abnormalities;Bonifas;Science,1991
5. Mapping of epidermolysis bullosa simplex mutation to chromosome 12;Ryynänen;Am J Human Genet,1991
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