Mutation in The Nuclear-Encoded Mitochondrial Isoleucyl-tRNA Synthetase IARS2 in Patients with Cataracts, Growth Hormone Deficiency with Short Stature, Partial Sensorineural Deafness, and Peripheral Neuropathy or with Leigh Syndrome [Human Mutation, 35(11), (2014) 1285-1289]

Human Mutation

Volumn 36, Issue 2, 2015, Pages 281-281

  Schwartzentruber, Jeremy ^a   Buhas, Daniela ^b   Majewski, Jacek ^a,c   Sasarman, Florin ^a   Papillon Cavanagh, Simon ^c   Thiffault, Isabelle ^a   Sheldon, Katherine M ^d   Massicotte, Christine ^e   Patry, Lysanne ^e   Simon, Mariella ^d   Zare, Amir S ^d   Mckernan, Kevin J ^d   Consortium, Forge Canada ^a   Michaud, Jacques ^e,f   Boles, Richard G ^d,g   Deal, Cheri L ^e   Desilets, Valerie ^e,f   Shoubridge, Eric A ^a   Samuels, Mark E ^e  

^a MCGILL UNIVERSITY   (Canada)

^b MONTREAL CHILDREN S HOSPITAL   (Canada)

^c MCGILL UNIVERSITY   (Canada)

^d University of Montreal ^*  (United States)

^e UNIVERSITY OF MONTREAL   (Canada)

^f UNIVERSITÉ DE MONTRÉAL   (Canada)

^g UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ERROR; PRIORITY JOURNAL;

EID: 84922015579     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.22756     Document Type: Article

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