Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the γ2 subunit of nicein/kalinin (LAMININ

Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the γ2 subunit of nicein/kalinin (LAMININ–5)

Published:1994-03 Issue:3 Volume:6 Page:299-304
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Aberdam Daniel,Galliano Marie-Florence,Vailly Joëlle,Pulkkinen Leena,Bonifas Jeannette,Christiano Angela M.,Tryggvason Karl,Uitto Jouni,Epstein Ervin H.,Ortonne Jean-Paul,Meneguzzi Guerrino

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0394-299.pdf

Reference36 articles.

1. Fine, J.D. et al. Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa. J. Am. Acad. Dermatol. 24, 119–135 (1991).

2. Epstein, E.H. Molecular genetics of epidermolysis bullosa. Science 256, 799–804 (1992).

3. Fine, J.D. Epidermolysis bullosa: clinical aspects, pathology and recent advances in research. Int. J. Dermatol. 25, 143–157 (1986).

4. Verrando, P. et al. Monoclonal antibody GB3, a new probe for the study of human basement membranes and hemidesmosomes. Exp. cell Res. 170, 116–128 (1987).

5. Kallunki, P. et al. A truncated laminin chain homologous to the B2 chain: structure, spatial expression and chromosomal assignement. J. cell Biol. 119, 679–693 (1992).

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