Genotype-phenotype correlation in Chinese patients with dystrophic epidermolysis bullosa pruriginosa

Acta Dermato-Venereologica

Volumn 92, Issue 1, 2012, Pages 50-53

  Jiang, Wei ^a   Sun, Ting Ting ^a   Lei, Peng Cheng ^a   Zhu, Xue Jun ^b  

^a PEKING UNIVERSITY THIRD HOSPITAL   (China)

^b PEKING UNIVERSITY FIRST HOSPITAL   (China)

Author keywords

Chinese patients; Dystrophic epidermolysis bullosa pruriginosa; Genotype phenotype correlation

Indexed keywords

CORTICOSTEROID; GLYCINE; THALIDOMIDE;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CHILD; CHINESE; CHINESE MEDICINE; CLINICAL ARTICLE; CLINICAL FEATURE; COL7A1 GENE; CONTROLLED STUDY; CORTICOSTEROID THERAPY; DYSTROPHIC EPIDERMOLYSIS BULLOSA PRURIGINOSA; EPIDERMOLYSIS BULLOSA DYSTROPHICA; EXON SKIPPING; FEMALE; GENE; GENE MUTATION; GENOTYPE PHENOTYPE CORRELATION; HUMAN; MALE; PRIORITY JOURNAL; PRURIGO; RNA SPLICING; SCHOOL CHILD; SKIN DEFECT; SKIN FRAGILITY; SKIN PRURITUS;

ADULT; AMINO ACID SUBSTITUTION; ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; CHINA; COLLAGEN TYPE VII; DNA MUTATIONAL ANALYSIS; EPIDERMOLYSIS BULLOSA DYSTROPHICA; EXONS; FEMALE; GENOTYPE; GLYCINE; HUMANS; MALE; MUTATION; PHENOTYPE; PRURIGO; RNA SPLICE SITES; RNA, MESSENGER; YOUNG ADULT;

EID: 84855233927     PISSN: 00015555     EISSN: None     Source Type: Journal    
DOI: 10.2340/00015555-1178     Document Type: Article

References (22)

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