| Literature DB >> 27426735 |
Robert Kopajtich1, Kei Murayama2, Andreas R Janecke3, Tobias B Haack1, Maximilian Breuer4, A S Knisely5, Inga Harting6, Toya Ohashi7, Yasushi Okazaki8, Daisaku Watanabe9, Yoshimi Tokuzawa10, Urania Kotzaeridou4, Stefan Kölker4, Sven Sauer4, Matthias Carl11, Simon Straub12, Andreas Entenmann12, Elke Gizewski13, René G Feichtinger14, Johannes A Mayr14, Karoline Lackner15, Tim M Strom1, Thomas Meitinger1, Thomas Müller12, Akira Ohtake16, Georg F Hoffmann4, Holger Prokisch1, Christian Staufner17.
Abstract
tRNA synthetase deficiencies are a growing group of genetic diseases associated with tissue-specific, mostly neurological, phenotypes. In cattle, cytosolic isoleucyl-tRNA synthetase (IARS) missense mutations cause hereditary weak calf syndrome. Exome sequencing in three unrelated individuals with severe prenatal-onset growth retardation, intellectual disability, and muscular hypotonia revealed biallelic mutations in IARS. Studies in yeast confirmed the pathogenicity of identified mutations. Two of the individuals had infantile hepatopathy with fibrosis and steatosis, leading in one to liver failure in the course of infections. Zinc deficiency was present in all affected individuals and supplementation with zinc showed a beneficial effect on growth in one.Entities:
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Year: 2016 PMID: 27426735 PMCID: PMC4974065 DOI: 10.1016/j.ajhg.2016.05.027
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025