Kindler syndrome: A focal adhesion genodermatosis

British Journal of Dermatology

Volumn 160, Issue 2, 2009, Pages 233-242

  Lai Cheong, J E ^a   Tanaka, A ^a   Hawche, G ^a   Emanuel, P ^b   Maari, C ^c   Taskesen, M ^d   Akdeniz, S ^d   Liu, L ^a   McGrath, J A ^a  

^a KING'S COLLEGE LONDON   (United Kingdom)

^b MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF MONTREAL   (Canada)

^d DICLE UNIVERSITY   (Turkey)

Author keywords

Actin; Blistering; Fermitin; FERMT1; Focal adhesion; Inherited skin disease; Poikiloderma

Indexed keywords

ACTIN; BETA1 INTEGRIN; BETA3 INTEGRIN;

AUTOSOMAL RECESSIVE DISORDER; CLINICAL FEATURE; CYTOSKELETON; DATA BASE; EPIDERMOLYSIS BULLOSA; EXTRACELLULAR MATRIX; FERMT1 GENE; FOCAL ADHESION; GASTROINTESTINAL DISEASE; GENE; GENE EXPRESSION; GENE IDENTIFICATION; GENE LOCATION; GENETIC HETEROGENEITY; GENODERMATOSIS; HISTOPATHOLOGY; HUMAN; KERATINOCYTE; KINDLER SYNDROME; LOSS OF FUNCTION MUTATION; NEOPLASM; PALLIATIVE THERAPY; PRIORITY JOURNAL; PROTEIN INTERACTION; REVIEW;

BLISTER; EPIDERMOLYSIS BULLOSA; EXTRACELLULAR MATRIX PROTEINS; FOCAL ADHESIONS; HUMANS; MEMBRANE PROTEINS; MUTATION; NEOPLASM PROTEINS; PERIODONTAL DISEASES; PHOTOSENSITIVITY DISORDERS; SYNDROME;

EID: 58349116039     PISSN: 00070963     EISSN: 13652133     Source Type: Journal    
DOI: 10.1111/j.1365-2133.2008.08976.x     Document Type: Review

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