A Keratin 14 Mutational Hot Spot for Epidermolysis Bullosa Simplex, Dowling-Meara: Implications for Diagnosis
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
Reference18 articles.
1. Sixteen types of epidermolysis bullosa: on the clinical discrimination, therapy and prenatal diagnosis;Gedde-Dahl;Acta Dermatol Venereol (suppl),1981
2. Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa;Fine;J Am Acad Dermatol,1991
3. Epidermolysis bullosa simplex: identification of a kindred with autosomal recessive transmission of the Weber-Cockayne variety;Fine;Pediatr Dermatol,1989
4. Epidermolysis bullosa resembling juvenile dermatitis herpetiformis;Dowling;Br J Derm,1954
5. Epidermolysis bullosa simplex: a new histologic subgroup;Nieme;Arch Dermatol,1983
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1. The Pathogenetic Role of IL-1β in Severe Epidermolysis Bullosa Simplex;Journal of Investigative Dermatology;2013-07
2. Defining Keratin Protein Function in Skin Epithelia: Epidermolysis Bullosa Simplex and Its Aftermath;Journal of Investigative Dermatology;2012-03
3. Localized Epidermolysis Bullosa Simplex (Weber-Cockayne type);Journal of Pediatric and Adolescent Gynecology;2011-12
4. Efficient KRT14 Targeting and Functional Characterization of Transplanted Human Keratinocytes for the Treatment of Epidermolysis Bullosa Simplex;Molecular Therapy;2010-09
5. 6 The vesiculobullous reaction pattern;Weedon's Skin Pathology;2010
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