Inherited epidermolysis bullosa

Orphanet Journal of Rare Diseases

Volumn 5, Issue 1, 2010, Pages

  Fine, Jo David ^a  

^a VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIGEN; CYTOKERATIN 14; CYTOKERATIN 5; KALININ; PLECTIN;

BLISTER; CLINICAL FEATURE; CONGENITAL DISORDER; DERMIS; DIAGNOSTIC PROCEDURE; DIFFERENTIAL DIAGNOSIS; DISEASE CLASSIFICATION; DNA DETERMINATION; EPIDERMOLYSIS BULLOSA; FAMILY HISTORY; GENE MUTATION; GENETIC COUNSELING; GENETICS; GRANULATION TISSUE; HEALTH; HUMAN; IMMUNOFLUORESCENCE; INJURY; KERATINOCYTE; MOUTH CAVITY; NUTRITION; ORGAN INJURY; POPULATION; PRENATAL DIAGNOSIS; PREVALENCE; PROGNOSIS; REVIEW; SKIN STRUCTURE; STAINING; TISSUE INJURY; TRANSMISSION ELECTRON MICROSCOPY; UNITED STATES; WOUND CARE;

EPIDERMOLYSIS BULLOSA; HUMANS;

EID: 77952687069     PISSN: None     EISSN: 17501172     Source Type: Journal    
DOI: 10.1186/1750-1172-5-12     Document Type: Review

References (84)

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