Molecular Consequences of Deletion of the Cytoplasmic Domain of Bullous Pemphigoid 180 in a Patient with Predominant Features of Epidermolysis Bullosa Simplex

Journal of Investigative Dermatology

Volumn 122, Issue 1, 2004, Pages 65-72

  Fontao, Lionel ^a   Tasanen, Kaisa ^b   Huber, Marcel ^c   Hohl, Daniel ^c   Koster, Jan ^d   Bruckner Tuderman, Leena ^e   Sonnenberg, Arnoud ^d   Borradori, Luca ^a,f  

^a UNIVERSITY HOSPITAL   (Switzerland)

^b UNIVERSITY OF OULU   (Finland)

^c LAUSANNE UNIVERSITY HOSPITAL   (Switzerland)

^d NETHERLANDS CANCER INSTITUTE   (Netherlands)

^e UNIVERSITY OF FREIBURG   (Germany)

^f GENEVA UNIVERSITY HOSPITALS   (Switzerland)

Author keywords

BP180; Collagen XVII; Epidermolysis bullosa; Hemidesmosome; Mutations

Indexed keywords

ASPARAGINE; ISOLEUCINE;

ARTICLE; BETA CHAIN; CELL STRAIN COS7; CLINICAL FEATURE; CONTROLLED STUDY; CYTOPLASM; DERMOEPIDERMAL JUNCTION; DESMOSOME; EPIDERMOLYSIS BULLOSA SIMPLEX; GENE DELETION; GENETIC LINKAGE; GENETIC TRANSFECTION; HETEROZYGOSITY; HUMAN; HUMAN CELL; HUMAN CELL CULTURE; INTERMEDIATE FILAMENT; KERATINOCYTE; MUTATIONAL ANALYSIS; PEMPHIGOID; PHENOTYPE; PRIORITY JOURNAL; PROTEIN ASSEMBLY; PROTEIN BINDING; PROTEIN DEGRADATION; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN STABILITY;

EID: 1642452817     PISSN: 0022202X     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.0022-202X.2003.22125.x     Document Type: Article

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