A novel frameshift mutation of the EDA1 gene in a Chinese Han family with X-linked hypohidrotic ectodermal dysplasia

Clinical and Experimental Dermatology

Volumn 34, Issue 1, 2009, Pages 74-76

  Zhang, H ^a,b   Quan, C ^a,b   Sun, L D ^a,b   Lv, H L ^a,b   Gao, M ^a,b   Zhou, F S ^b   Xiao, F L ^a,b   Fang, Q Y ^b   Shen, Y J ^b   Zhou, L ^c   Yang, S ^a,b   Zhang, X J ^a,b  

^a ANHUI MEDICAL UNIVERSITY   (China)

^b BEIJING UNIVERSITY OF POSTS AND TELECOMMUNICATIONS   (China)

^c UNIVERSITY OF MISSISSIPPI MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHINESE; CLINICAL FEATURE; DISEASE ASSOCIATION; ECTODERMAL DYSPLASIA; EDA1 GENE; FRAMESHIFT MUTATION; GENE; GENE DELETION; GENE SEQUENCE; HUMAN; LABORATORY TEST; MALE; MISSENSE MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; STOP CODON; X CHROMOSOME LINKED DISORDER;

ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; DNA MUTATIONAL ANALYSIS; ECTODERMAL DYSPLASIA 1, ANHIDROTIC; ECTODYSPLASINS; EXONS; FRAMESHIFT MUTATION; HUMANS; MALE; PEDIGREE; SEQUENCE DELETION; YOUNG ADULT;

EID: 57349114238     PISSN: 03076938     EISSN: 13652230     Source Type: Journal    
DOI: 10.1111/j.1365-2230.2008.02844.x     Document Type: Article

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