A dinucleotide mutation in the endothelin-B receptor gene is associated with lethal white foal syndrome (LWFS); a horse variant of Hirschsprung disease (HSCR)

Human Molecular Genetics

Volumn 7, Issue 6, 1998, Pages 1047-1052

  Yang, G C ^a   Croaker, D ^a   Zhang, A L ^a   Manglick, P ^a   Cartmill, T ^a   Cass, D ^a  

^a CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; DINUCLEOTIDE; DNA FRAGMENT; ENDOTHELIN A RECEPTOR; ENDOTHELIN B RECEPTOR; ISOLEUCINE; LYSINE; MEMBRANE PROTEIN;

AMINO ACID SEQUENCE; ANIMAL CELL; ARTICLE; CONTROLLED STUDY; GENE MUTATION; HIRSCHSPRUNG DISEASE; HORSE DISEASE; NONHUMAN; OPEN READING FRAME; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN DOMAIN; RECEPTOR GENE; SEQUENCE ANALYSIS;

ANIMALS; DNA MUTATIONAL ANALYSIS; DNA, COMPLEMENTARY; HIRSCHSPRUNG DISEASE; HORSE DISEASES; HORSES; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION; NUCLEOTIDES; RECEPTOR, ENDOTHELIN B; RECEPTORS, ENDOTHELIN; SEQUENCE HOMOLOGY, AMINO ACID;

ANIMALIA; BOVINAE; EQUIDAE; EQUUS CABALLUS; RODENTIA;

EID: 0031831546     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/7.6.1047     Document Type: Article

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