Epidermolysis bullosa simplex in Scotland caused by a spectrum of keratin mutations

Journal of Investigative Dermatology

Volumn 127, Issue 3, 2007, Pages 574-580

  Rugg, Elizabeth L ^a,d   Horn, Helen M ^b   Smith, Frances J ^a,c   Wilson, Neil J ^a   Hill, Alison J M ^a   Magee, Gareth J ^a   Shemanko, Carrie S ^a,e   Baty, David U ^c   Tidman, Michael J ^a   Lane, E Birgitte ^a,f  

^a UNIVERSITY OF DUNDEE   (United Kingdom)

^b ROYAL INFIRMARY OF EDINBURGH   (United Kingdom)

^c UNIVERSITY OF DUNDEE   (United Kingdom)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e UNIVERSITY OF CALGARY   (Canada)

^f AGENCY FOR SCIENCE   (Singapore)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOKERATIN 14; CYTOKERATIN 5;

ADOLESCENT; ADULT; AGED; ARTICLE; BLISTER; BULLOUS SKIN DISEASE; CHILD; CONTROLLED STUDY; CYTOLYSIS; DISEASE SEVERITY; EPIDERMOLYSIS BULLOSA SIMPLEX; GENE MUTATION; HUMAN; KERATINOCYTE; MAJOR CLINICAL STUDY; PHENOTYPE; PRIORITY JOURNAL; SYMPTOM;

EID: 33847014854     PISSN: 0022202X     EISSN: 15231747     Source Type: Journal    
DOI: 10.1038/sj.jid.5700571     Document Type: Article

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