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- Q64040502 description "article scientifique publié en 2019" @default.
- Q64040502 description "artículu científicu espublizáu en febreru de 2019" @default.
- Q64040502 description "im Mai 2019 veröffentlichter wissenschaftlicher Artikel" @default.
- Q64040502 description "scientific article published on 17 February 2019" @default.
- Q64040502 description "wetenschappelijk artikel" @default.
- Q64040502 description "наукова стаття, опублікована в травні 2019" @default.
- Q64040502 name "Homozygous variant in OTX2 and possible genetic modifiers identified in a patient with combined pituitary hormone deficiency, ocular involvement, myopathy, ataxia, and mitochondrial impairment" @default.
- Q64040502 name "Homozygous variant in OTX2 and possible genetic modifiers identified in a patient with combined pituitary hormone deficiency, ocular involvement, myopathy, ataxia, and mitochondrial impairment" @default.
- Q64040502 type Item @default.
- Q64040502 label "Homozygous variant in OTX2 and possible genetic modifiers identified in a patient with combined pituitary hormone deficiency, ocular involvement, myopathy, ataxia, and mitochondrial impairment" @default.
- Q64040502 label "Homozygous variant in OTX2 and possible genetic modifiers identified in a patient with combined pituitary hormone deficiency, ocular involvement, myopathy, ataxia, and mitochondrial impairment" @default.
- Q64040502 prefLabel "Homozygous variant in OTX2 and possible genetic modifiers identified in a patient with combined pituitary hormone deficiency, ocular involvement, myopathy, ataxia, and mitochondrial impairment" @default.
- Q64040502 prefLabel "Homozygous variant in OTX2 and possible genetic modifiers identified in a patient with combined pituitary hormone deficiency, ocular involvement, myopathy, ataxia, and mitochondrial impairment" @default.
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- Q64040502 P356 Q64040502-22EB7230-2C9A-4103-9B9D-B79D9844E347 @default.
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- Q64040502 P921 Q64040502-CE6473BB-366C-4D32-9FAE-FF7987C4E107 @default.
- Q64040502 P356 AJMG.A.61092 @default.
- Q64040502 P698 30773800 @default.
- Q64040502 P1433 Q4744254 @default.
- Q64040502 P1476 "Homozygous variant in OTX2 and possible genetic modifiers identified in a patient with combined pituitary hormone deficiency, ocular involvement, myopathy, ataxia, and mitochondrial impairment" @default.
- Q64040502 P2093 "Alessia Catania" @default.
- Q64040502 P2093 "Costanza Lamperti" @default.
- Q64040502 P2093 "Lorenzo Nanetti" @default.
- Q64040502 P2093 "Lorenzo Peverelli" @default.
- Q64040502 P2093 "Nadia Zanetti" @default.
- Q64040502 P304 "827-831" @default.
- Q64040502 P31 Q13442814 @default.
- Q64040502 P356 "10.1002/AJMG.A.61092" @default.
- Q64040502 P407 Q1860 @default.
- Q64040502 P433 "5" @default.
- Q64040502 P478 "179" @default.
- Q64040502 P50 Q30093362 @default.
- Q64040502 P50 Q55712561 @default.
- Q64040502 P50 Q58242359 @default.
- Q64040502 P577 "2019-02-17T00:00:00Z" @default.
- Q64040502 P698 "30773800" @default.
- Q64040502 P921 Q114049690 @default.