Mutation analysis and molecular genetics of epidermolysis bullosa-Reference-Cited by-同舟云学术

Mutation analysis and molecular genetics of epidermolysis bullosa

Published:1999-02 Issue:1 Volume:18 Page:29-42
ISSN:0945-053X
Container-title:Matrix Biology
language:en
Short-container-title:Matrix Biology

Author:

Pulkkinen Leena,Uitto Jouni

Publisher

Elsevier BV

Subject

Molecular Biology

Reference91 articles.

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3. Bruckner-Tuderman, L., 1993. Epidermolysisi bullosa. In: Royce, P.M., Steinmann, B. (Eds.), Connective Tissue and its Heritable Disorders: Molecular, Genetic and Medical Aspects. Wiley-Liss, New York, pp. 507–532.

4. Anchoring fibrils and type VII collagen are absent from skin in severe recessive dystrophic epidermolysis bullosa;Bruckner-Tuderman;J. Invest. Dermatol.,1989

5. Type VII collagen, anchoring fibrils, and epidermolysis bullosa;Burgeson;J. Invest. Dermatol.,1993

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