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
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| Description | scientific article |
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author: Mariella Simon Simon Papillon-Cavanagh Jacques L. Michaud Jeremy Schwartzentruber Jacek Majewski FORGE Canada Kevin McKernan |
| Publication date | October 18, 2014 |
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