Epidermolysis Bullosa Simplex (Dowling-Meara Type) Is a Genetic Disease Characterized by an Abnormal Keratin-Filament Network Involving Keratins K5 and K14-Reference-Cited by-同舟云学术

Epidermolysis Bullosa Simplex (Dowling-Meara Type) Is a Genetic Disease Characterized by an Abnormal Keratin-Filament Network Involving Keratins K5 and K14

Published:1991-12 Issue:6 Volume:97 Page:959-968
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Ishida-Yamamoto Akemi,McGrath John A,Chapman Stephen J,Leigh Iren M,Lane E Birgitte,Eady Robin A J

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference54 articles.

1. Epidermolysis bullosa resembling juvenile dermatitis herpetiformis;Dowling;Br J Dermatol,1954

2. Epidermolysis bullosa herpetiformis Dowling-Meara. Report of a case and pathomorphogenesis;Anton-Lamprecht;Dermatologica,1982

3. Epidermolysis bullosa simplex. A new histologic subgroup;Niemi;Arch Dermatol,1983

4. Severe infantile epidermolysis bullosa simplex. Dowling-Meara type;Buchbinder;Arch Dermatol,1986

5. Keratin expression in epidermolysis bullosa simplex (Dowling-Meara);Tidman;Arch Derm Venereol,1988

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