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- Q57263414 description "2015 ഫെബ്രുവരി 1 നു പ്രസിദ്ധീകരിച്ച ശാസ്ത്ര ലേഖനം" @default.
- Q57263414 description "article scientifique publié en 2015" @default.
- Q57263414 description "article" @default.
- Q57263414 description "artículu científicu" @default.
- Q57263414 description "im Februar 2015 veröffentlichter wissenschaftlicher Artikel" @default.
- Q57263414 description "wetenschappelijk artikel" @default.
- Q57263414 description "наукова стаття, опублікована в лютому 2015" @default.
- Q57263414 name "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" @default.
- Q57263414 name "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" @default.
- Q57263414 type Item @default.
- Q57263414 label "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" @default.
- Q57263414 label "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" @default.
- Q57263414 prefLabel "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" @default.
- Q57263414 prefLabel "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" @default.
- Q57263414 P1433 Q57263414-2C918979-7113-4A06-BB9B-FDA0B9ACD2FF @default.
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- Q57263414 P478 Q57263414-A4C7D764-D4F7-485A-B5B5-9546C6AAFACC @default.
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- Q57263414 P577 Q57263414-DAF2F38F-E79F-495F-B78C-9779804F3E69 @default.
- Q57263414 P921 Q57263414-970D03EB-FB38-4A32-AB60-F6C2EC3240AA @default.
- Q57263414 P921 Q57263414-ABE56151-C655-4643-864A-003A8BDA6826 @default.
- Q57263414 P921 Q57263414-B0A342D0-12E5-406D-A327-011849F6F4AD @default.
- Q57263414 P356 HUMU.22756 @default.
- Q57263414 P1433 Q5937269 @default.
- Q57263414 P1476 "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" @default.
- Q57263414 P2093 "Amir S. Zare" @default.
- Q57263414 P2093 "Cheri L. Deal" @default.
- Q57263414 P2093 "Christine Massicotte" @default.
- Q57263414 P2093 "Daniela Buhas" @default.
- Q57263414 P2093 "Eric A. Shoubridge" @default.
- Q57263414 P2093 "FORGE Canada Consortium" @default.
- Q57263414 P2093 "Florin Sasarman" @default.
- Q57263414 P2093 "Isabelle Thiffault" @default.
- Q57263414 P2093 "Jacek Majewski" @default.
- Q57263414 P2093 "Jeremy Schwartzentruber" @default.
- Q57263414 P2093 "Katherine M. Sheldon" @default.
- Q57263414 P2093 "Lysanne Patry" @default.
- Q57263414 P2093 "Mariella Simon" @default.
- Q57263414 P2093 "Mark E. Samuels" @default.
- Q57263414 P2093 "Richard G. Boles" @default.
- Q57263414 P2093 "Simon Papillon-Cavanagh" @default.
- Q57263414 P2093 "Valerie Desilets" @default.
- Q57263414 P304 "281-281" @default.
- Q57263414 P31 Q13442814 @default.
- Q57263414 P356 "10.1002/HUMU.22756" @default.
- Q57263414 P433 "2" @default.
- Q57263414 P478 "36" @default.
- Q57263414 P50 Q102286139 @default.
- Q57263414 P50 Q30361559 @default.
- Q57263414 P577 "2015-02-01T00:00:00Z" @default.
- Q57263414 P921 Q12133 @default.
- Q57263414 P921 Q369262 @default.
- Q57263414 P921 Q945238 @default.