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Wiley, Human Mutation: Variation, Informatics and Disease, 2(36), p. 281-281, 2015

DOI: 10.1002/humu.22756

Wiley, Human Mutation: Variation, Informatics and Disease, p. n/a-n/a, 2014

DOI: 10.1002/humu.22629

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Mutation in The Nuclear-Encoded Mitochondrial Isoleucyl-tRNA SynthetaseIARS2in Patients with Cataracts, Growth Hormone Deficiency with Short Stature, Partial Sensorineural Deafness, and Peripheral Neuropathy or with Leigh Syndrome

Journal article published in 2015 by Jeremy Schwartzentruber, Daniela Buhas, Jacek Majewski, Florin Sasarman, Simon Papillon-Cavanagh, Isabelle Thiffault, Katherine M. Sheldon, Christine Massicotte, Lysanne Patry, Mariella Simon, Amir S. Zare, Kevin J. McKernan ORCID, Forge Canada Consortium, Jacques Michaud, Richard G. Boles and other authors.
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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