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- Q91511417 description "artículu científicu espublizáu en payares de 2019" @default.
- Q91511417 description "im November 2019 veröffentlichter wissenschaftlicher Artikel" @default.
- Q91511417 description "scientific article published on 26 November 2019" @default.
- Q91511417 description "wetenschappelijk artikel" @default.
- Q91511417 description "наукова стаття, опублікована 26 листопада 2019" @default.
- Q91511417 name "Whole exome sequencing identifies a homozygous POLG2 missense variant in an adult patient presenting with optic atrophy, movement disorders, premature ovarian failure and mitochondrial DNA depletion" @default.
- Q91511417 name "Whole exome sequencing identifies a homozygous POLG2 missense variant in an adult patient presenting with optic atrophy, movement disorders, premature ovarian failure and mitochondrial DNA depletion" @default.
- Q91511417 type Item @default.
- Q91511417 label "Whole exome sequencing identifies a homozygous POLG2 missense variant in an adult patient presenting with optic atrophy, movement disorders, premature ovarian failure and mitochondrial DNA depletion" @default.
- Q91511417 label "Whole exome sequencing identifies a homozygous POLG2 missense variant in an adult patient presenting with optic atrophy, movement disorders, premature ovarian failure and mitochondrial DNA depletion" @default.
- Q91511417 prefLabel "Whole exome sequencing identifies a homozygous POLG2 missense variant in an adult patient presenting with optic atrophy, movement disorders, premature ovarian failure and mitochondrial DNA depletion" @default.
- Q91511417 prefLabel "Whole exome sequencing identifies a homozygous POLG2 missense variant in an adult patient presenting with optic atrophy, movement disorders, premature ovarian failure and mitochondrial DNA depletion" @default.
- Q91511417 P1433 Q91511417-05A18728-2EE3-4507-A282-C79D65A7D72A @default.
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- Q91511417 P31 Q91511417-546E2447-C575-4C4B-8EE0-803474DC854A @default.
- Q91511417 P356 Q91511417-55101B8B-61D5-4BA9-B1C8-E754642A19B2 @default.
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- Q91511417 P50 Q91511417-D38FCB77-FE06-47ED-AAA8-8867D351AE59 @default.
- Q91511417 P50 Q91511417-E148706A-CE7F-492C-A64B-B1FC0201A6F3 @default.
- Q91511417 P50 Q91511417-F5CE0E25-9BE6-49B0-B6F1-29FB0325FD5F @default.
- Q91511417 P577 Q91511417-109763AA-89B4-4A4D-9492-3B7B4ED16F2A @default.
- Q91511417 P698 Q91511417-EEDC4E45-F0D0-42AE-9C2D-CCDA0172F2E5 @default.
- Q91511417 P921 Q91511417-26BA995B-9FBF-48BB-8934-546E1604A38A @default.
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- Q91511417 P921 Q91511417-A35628C8-A743-4B33-824F-353E683302F6 @default.
- Q91511417 P356 J.EJMG.2019.103821 @default.
- Q91511417 P698 31778857 @default.
- Q91511417 P1433 Q15817083 @default.
- Q91511417 P1476 "Whole exome sequencing identifies a homozygous POLG2 missense variant in an adult patient presenting with optic atrophy, movement disorders, premature ovarian failure and mitochondrial DNA depletion" @default.
- Q91511417 P2093 "Alexandra Mosejova" @default.
- Q91511417 P2093 "Magdalena Kaliszewska" @default.
- Q91511417 P2093 "Matej Skorvanek" @default.
- Q91511417 P2093 "Miriam Skirkova" @default.
- Q91511417 P2093 "Petra Dosekova" @default.
- Q91511417 P2093 "Victor Murcia Pienkowski" @default.
- Q91511417 P2093 "Viera Habalova" @default.
- Q91511417 P2093 "Vladimir Han" @default.
- Q91511417 P2093 "Zuzana Gdovinova" @default.
- Q91511417 P2860 Q53612457 @default.
- Q91511417 P304 "103821" @default.
- Q91511417 P31 Q13442814 @default.
- Q91511417 P356 "10.1016/J.EJMG.2019.103821" @default.
- Q91511417 P433 "4" @default.
- Q91511417 P478 "63" @default.
- Q91511417 P50 Q42684599 @default.
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- Q91511417 P50 Q89348616 @default.
- Q91511417 P577 "2019-11-26T00:00:00Z" @default.
- Q91511417 P698 "31778857" @default.
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