A mutational hot spot in keratin 10 (KRT 10) in patients with epidermolytic hyperkeratosis

Human Molecular Genetics

Volumn 2, Issue 12, 1993, Pages 2147-2150

  Rothnagel, Joseph A ^a   Fisher, Monte P ^a   Axtell, Shelli M ^a   Pittelkow, Mark R ^b   Anton lamprecht, Ingrun ^c   Huber, Marcel ^d   Hohl, Daniel ^d   Roop, Dennis R ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b MAYO CLINIC   (United States)

^c UNIVERSITY OF HEIDELBERG   (Germany)

^d LAUSANNE UNIVERSITY HOSPITAL   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

KERATIN;

AMINO ACID SUBSTITUTION; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DNA SEQUENCE; FEMALE; GENE MUTATION; HUMAN; HYPERKERATOSIS; MALE; PRIORITY JOURNAL; PROTEIN DOMAIN; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

AMINO ACID SEQUENCE; ARGININE; BASE SEQUENCE; DNA PRIMERS; HYPERKERATOSIS, EPIDERMOLYTIC; KERATIN; MOLECULAR SEQUENCE DATA; POINT MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM (GENETICS); PROTEIN STRUCTURE, SECONDARY; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0027742236     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/2.12.2147     Document Type: Note

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