Epidermolysis Bullosa Simplex with Mottled Pigmentation: A Family Report and Review-Reference-Cited by-同舟云学术

Epidermolysis Bullosa Simplex with Mottled Pigmentation: A Family Report and Review

Published:2012-05-29 Issue:6 Volume:30 Page:e125-e131
ISSN:0736-8046
Container-title:Pediatric Dermatology
language:en
Short-container-title:Pediatr Dermatol

Author:

Echeverría-García Begoña,Vicente Asunción,Hernández Ángela,Mascaró Jose M.,Colmenero Isabel,Terrón Ana,Escámez María J.,del Río Marcela,González-Enseñat Maria A.,Torrelo Antonio

Publisher

Wiley

Subject

Dermatology,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1525-1470.2012.01748.x/fullpdf

Reference28 articles.

1. Epidermolysis bullosa simplex and mottled pigmentation: a new dominant syndrome. I. Clinical and histological features;Fischer;Clin Genet,1979

2. Epidermolysis bullosa simplex with mottled pigmentation: clinical aspects and confirmation of the P24L mutation in the KRT5 gene in further patients;Moog;Am J Med Genet,1999

3. Epidermolysis bullosa simplex with mottled pigmentation;Bruckner-Tuderman;J Am Acad Dermatol,1989

4. Two novel recessive mutations in KRT14 identified in a cohort of 21 Spanish families with epidermolysis bullosa simplex;García;Br J Dermatol,2011

5. The genetic basis of epidermolysis bullosa simplex with mottled pigmentation;Uttam;Proc Natl Acad Sci U S A,1996

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