Inherited epidermolysis bullosa: Updated recommendations on diagnosis and classification-Reference-Cited by-同舟云学术

Inherited epidermolysis bullosa: Updated recommendations on diagnosis and classification

Published:2014-06 Issue:6 Volume:70 Page:1103-1126
ISSN:0190-9622
Container-title:Journal of the American Academy of Dermatology
language:en
Short-container-title:Journal of the American Academy of Dermatology

Author:

Fine Jo-David,Bruckner-Tuderman Leena,Eady Robin A.J.,Bauer Eugene A.,Bauer Johann W.,Has Cristina,Heagerty Adrian,Hintner Helmut,Hovnanian Alain,Jonkman Marcel F.,Leigh Irene,Marinkovich M. Peter,Martinez Anna E.,McGrath John A.,Mellerio Jemima E.,Moss Celia,Murrell Dedee F.,Shimizu Hiroshi,Uitto Jouni,Woodley David,Zambruno Giovanna

Publisher

Elsevier BV

Subject

Dermatology

Reference32 articles.

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4. A homozygous nonsense mutation in the human desmocollin-3 (DSC3) gene underlies hereditary hypotrichosis and recurrent skin vesicles;Ayub;Am J Hum Genet,2009

5. No evidence of skin blisters with human desmocollin-3 gene mutation;Payne;Am J Hum Genet,2010

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