The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains

Proceedings of the National Academy of Sciences of the United States of America

Volumn 94, Issue 24, 1997, Pages 13069-13074

  Srivastava, Anand K ^a   Pispa, Johanna ^b   Hartung, Andrew J ^a   Du, Yangzhu ^a   Ezer, Sini ^b   Jenks, Ted ^a   Shimada, Tokihiko ^c   Pekkanen, Maija ^b   Mikkola, Marja L ^b   Ko, Minoru S H ^c   Thesleff, Irma ^b   Kere, Juha ^b   Schlessinger, David ^d  

^a GREENWOOD GENETIC CENTER   (United States)

^b UNIVERSITY OF HELSINKI   (Finland)

^c WAYNE STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; ECTODYSPLASIN A; MEMBRANE PROTEIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; EPIDERMIS CELL; GENE DELETION; GENE EXPRESSION; GENE ISOLATION; HUMAN; HUMAN CELL; MOLECULAR CLONING; MOUSE; NONHUMAN; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL; TOOTH DEVELOPMENT; X CHROMOSOME LINKAGE;

ALTERNATIVE SPLICING; AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; DNA, COMPLEMENTARY; ECTODYSPLASINS; EXONS; HOMEODOMAIN PROTEINS; HUMANS; MEMBRANE PROTEINS; MICE; MOLECULAR SEQUENCE DATA; MUTATION; NEUROPEPTIDES; PHENOTYPE; PROMOTER REGIONS (GENETICS); SEQUENCE HOMOLOGY, AMINO ACID;

ANIMALIA;

EID: 12644310324     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.94.24.13069     Document Type: Article

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