A missense mutation in the endothelin-B receptor gene is associated with Lethal White Foal Syndrome: An equine version of Hirschsprung Disease

Mammalian Genome

Volumn 9, Issue 6, 1998, Pages 426-431

  Metallinos, D L ^a,b   Bowling, A T ^b   Rine, J ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ENDOTHELIN B RECEPTOR;

ANIMAL CELL; ARTICLE; GENETIC ASSOCIATION; HIRSCHSPRUNG DISEASE; HOMOZYGOSITY; HORSE; HUMAN; HUMAN CELL; LETHAL WHITE FOAL SYNDROME; MISSENSE MUTATION; NONHUMAN; RECEPTOR BINDING; RECEPTOR GENE;

ALLELES; AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CLONING, MOLECULAR; CONSENSUS SEQUENCE; HIRSCHSPRUNG DISEASE; HORSE DISEASES; HORSES; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION; OPEN READING FRAMES; RECEPTOR, ENDOTHELIN B; RECEPTORS, ENDOTHELIN; SEQUENCE ALIGNMENT;

ANIMALIA; EQUIDAE; EQUUS CABALLUS;

EID: 0031828292     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003359900790     Document Type: Article

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