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...

תיאור מלא

שמור ב:
מידע ביבליוגרפי
Main Authors: Hirano, Takashi, Kobayashi, Naohiko, Matsuhashi, Tamako, Watanabe, Daisaku, Watanabe, Toshio, Takasuga, Akiko, Sugimoto, Mayumi, Sugimoto, Yoshikazu
פורמט: Artigo
שפה:Inglês
יצא לאור: Public Library of Science 2013
נושאים:
Research Article
גישה מקוונת: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
תגים: הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!

פריטים דומים