Epidermolysis bullosa: a spectrum of clinical phenotypes explained by molecular heterogeneity
Author:
Publisher
Elsevier BV
Subject
Genetics,Molecular Medicine
Reference45 articles.
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3. Plectin and human genetic disorders of skin and muscle. The paradigm of epidermolysis bullosa with muscular dystrophy;Uitto;Exp. Dermatol.,1996
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5. Cloning of type XVII collagen. Complementary and genomic DNA sequences of mouse 180-kilodalton bullous pemphigoid antigen (BPAG2) predict an interrupted collagenous domain, a transmembrane segment, and unusual features in the 5‘-end of the gene and the 3‘-untranslated region of the mRNA.
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