Arachnomelia syndrome in Simmental cattle is caused by a homozygous 2-bp deletion in the molybdenum cofactor synthesis step 1 gene (MOCS1)

BMC Genetics

Volumn 12, Issue , 2011, Pages

  Buitkamp, Johannes ^a   Semmer, Jördis ^a   Götz, Kay Uwe ^a  

^a Bundesforschungsanstalt fü Landwirtschaft   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARACHNOMELIA SYNDROME; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CATTLE; CATTLE DISEASE; GENE; GENE DELETION; GENE IDENTIFICATION; GENE MAPPING; GENE MUTATION; GENOTYPE; HETEROZYGOTE; MOLYBDENUM COFACTOR SYNTHESIS STEP 1 GENE; NONHUMAN; ANIMAL; ANIMAL DISEASE; CHROMOSOME MAP; COENZYME; GENETICS; HOMOZYGOTE; MUSCULOSKELETAL SYSTEM MALFORMATION; SYNDROME;

BOS; BOVINAE;

METALLOPROTEIN; MOLYBDENUM COFACTOR; PTERIDINE DERIVATIVE;

ANIMALS; CATTLE; CATTLE DISEASES; CHROMOSOME MAPPING; COENZYMES; GENE DELETION; HOMOZYGOTE; METALLOPROTEINS; MUSCULOSKELETAL ABNORMALITIES; PTERIDINES; SYNDROME;

EID: 78651548068     PISSN: None     EISSN: 14712156     Source Type: Journal    
DOI: 10.1186/1471-2156-12-11     Document Type: Article

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