Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterization-Reference-Cited by-同舟云学术

Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterization

Published:2006-08-17 Issue:4 Volume:70 Page:339-347
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Drera B,Castiglia D,Zoppi N,Gardella R,Tadini G,Floriddia G,De Luca N,Pedicelli C,Barlati S,Zambruno G,Colombi M

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2006.00679.x/fullpdf

Reference32 articles.

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2. Inherited epidermolysis bullosa comes into the new millennium: a revised classification system based on current knowledge of pathogenetic mechanisms and the clinical, laboratory, and epidemiologic findings of large, well-defined patient cohorts;Fine;J Am Acad Dermatol,2000

3. Human type VII collagen: genetic linkage of the gene (COL7A1) on chromosome 3 to dominant dystrophic epidermolysis bullosa;Ryynanen;Am J Hum Genet,1991

4. Molecular basis of dystrophic epidermolysis bullosa: mutations in the type VII collagen gene (COL7A1);Järvikallio;Hum Mutat,1997

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