Keratin 1 and keratin 10 mutations causing epidermolytic hyperkeratosis in Chinese patients

Journal of Dermatological Science

Volumn 29, Issue 3, 2002, Pages 195-200

  Sun, Xiukun ^a   Ma, Linglei ^a   Xie, Yanqiu ^a   Zhu, Xuejun ^a  

^a PEKING UNIVERSITY FIRST HOSPITAL   (China)

Author keywords

Epidermolytic hyperkeratosis; Keratin 1; Keratin 10; Mutation

Indexed keywords

DNA; KERATIN; KERATIN 10; KERATIN TYPE 1; UNCLASSIFIED DRUG;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CHILD; CHINESE; CLINICAL ARTICLE; CODON; CORRELATION ANALYSIS; FAMILIAL DISEASE; FEMALE; GENE MUTATION; GENETIC VARIABILITY; HUMAN; HYPERKERATOSIS; KERATOSIS PALMOPLANTARIS; MALE; MUTATIONAL ANALYSIS; PHENOTYPIC VARIATION; POINT MUTATION; PRIORITY JOURNAL;

ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; FEMALE; HUMANS; HYPERKERATOSIS, EPIDERMOLYTIC; INFANT; KERATIN-10; KERATINS; MALE; MOLECULAR SEQUENCE DATA; MUTATION; SKIN;

EID: 0036758439     PISSN: 09231811     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0923-1811(02)00040-3     Document Type: Article

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