Mapping and Exome Sequencing Identifies a Mutation in the IARS Gene as the Cause of Hereditary Perinatal Weak Calf Syndrome

We identified an IARS (isoleucyl-tRNA synthetase) c.235G>C (p.Val79Leu) substitution as the causative mutation for neonatal weakness with intrauterine growth retardation (perinatal weak calf syndrome). In Japanese Black cattle, the syndrome was frequently found in calves sired by Bull A. Hence, w...

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Main Authors: Hirano, Takashi, Kobayashi, Naohiko, Matsuhashi, Tamako, Watanabe, Daisaku, Watanabe, Toshio, Takasuga, Akiko, Sugimoto, Mayumi, Sugimoto, Yoshikazu
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2013
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3660308/
https://ncbi.nlm.nih.gov/pubmed/23700453
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0064036
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