Recurrent R156H mutation of KRT10 in a Japanese family with bullous congenital ichthyosiform erythroderma

Journal of the European Academy of Dermatology and Venereology

Volumn 14, Issue 4, 2000, Pages 304-306

  Mayuzumi, N ^a   Shigihara, T ^a   Ikeda, S ^a   Ogawa, H ^a  

^a JUNTENDO UNIVERSITY   (Japan)

Author keywords

BCIE; KRT10

Indexed keywords

AMINO ACID; ARGININE; DNA; HISTIDINE; KERATIN; KERATIN 10; UNCLASSIFIED DRUG;

AMINO ACID SUBSTITUTION; ARTICLE; BULLOUS SKIN DISEASE; CODON; CONGENITAL ICHTHYOSIFORM ERYTHRODERMA; CONTROLLED STUDY; DNA DETERMINATION; ELECTROPHORESIS; FAMILY STUDY; GENE MUTATION; HUMAN; HUMAN CELL; HUMAN TISSUE; JAPAN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

AMINO ACID SUBSTITUTION; CODON; FEMALE; HUMANS; HYPERKERATOSIS, EPIDERMOLYTIC; JAPAN; KERATINS; MALE; MUTATION; PEDIGREE;

EID: 0034426618     PISSN: 09269959     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1468-3083.2000.00101.x     Document Type: Article

References (15)

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