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- Q96123479 description "article scientifique publié en 2020" @default.
- Q96123479 description "artículu científicu espublizáu n'abril de 2020" @default.
- Q96123479 description "im April 2020 veröffentlichter wissenschaftlicher Artikel" @default.
- Q96123479 description "scientific article published on 15 April 2020" @default.
- Q96123479 description "wetenschappelijk artikel" @default.
- Q96123479 description "наукова стаття, опублікована 15 квітня 2020" @default.
- Q96123479 name "Mitochondrial DNA depletion syndrome in a newborn with Jaundice Caused by DGUOK mutation and complete uniparental disomy of chromosome 2" @default.
- Q96123479 name "Mitochondrial DNA depletion syndrome in a newborn with Jaundice Caused by DGUOK mutation and complete uniparental disomy of chromosome 2" @default.
- Q96123479 type Item @default.
- Q96123479 label "Mitochondrial DNA depletion syndrome in a newborn with Jaundice Caused by DGUOK mutation and complete uniparental disomy of chromosome 2" @default.
- Q96123479 label "Mitochondrial DNA depletion syndrome in a newborn with Jaundice Caused by DGUOK mutation and complete uniparental disomy of chromosome 2" @default.
- Q96123479 prefLabel "Mitochondrial DNA depletion syndrome in a newborn with Jaundice Caused by DGUOK mutation and complete uniparental disomy of chromosome 2" @default.
- Q96123479 prefLabel "Mitochondrial DNA depletion syndrome in a newborn with Jaundice Caused by DGUOK mutation and complete uniparental disomy of chromosome 2" @default.
- Q96123479 P1433 Q96123479-2BBC5600-CC0A-4B97-A47B-5DD432BA710F @default.
- Q96123479 P1476 Q96123479-443D4872-6C81-4FB1-BCDB-D41D1D7EFFB9 @default.
- Q96123479 P2093 Q96123479-57F4DEB0-0700-4AFF-BA02-B5AAB0E4E799 @default.
- Q96123479 P2093 Q96123479-5ED5ADCD-9CFF-40AE-A6A5-BE276D0C6B91 @default.
- Q96123479 P2093 Q96123479-79C7F8D1-60EF-4442-A81C-FC77A0542FC4 @default.
- Q96123479 P2093 Q96123479-7B3BB51B-BF21-4ACD-94D5-76760EB6959C @default.
- Q96123479 P2093 Q96123479-AD43907C-6D8F-42CB-BA6E-839F6E14E5B5 @default.
- Q96123479 P2093 Q96123479-AE7A1EBB-F44A-4650-93DB-D41FB1C11183 @default.
- Q96123479 P31 Q96123479-87743AAA-9100-45B7-BCAA-84FF47D0B350 @default.
- Q96123479 P356 Q96123479-CF8B3555-E1C1-4F40-A340-56401236D80B @default.
- Q96123479 P577 Q96123479-CA5DA258-5772-4499-8F1E-F69E9D0028C3 @default.
- Q96123479 P698 Q96123479-65156A63-B8B1-48D2-A0D5-C444E00B0968 @default.
- Q96123479 P921 Q96123479-3031B300-1CE9-4E10-B215-935AB2F882EE @default.
- Q96123479 P356 J.PEDNEO.2020.04.005 @default.
- Q96123479 P698 32482602 @default.
- Q96123479 P1433 Q26853906 @default.
- Q96123479 P1476 "Mitochondrial DNA depletion syndrome in a newborn with Jaundice Caused by DGUOK mutation and complete uniparental disomy of chromosome 2" @default.
- Q96123479 P2093 "Chen Chen" @default.
- Q96123479 P2093 "Jing-Jing Meng" @default.
- Q96123479 P2093 "Jun-Ke Xia" @default.
- Q96123479 P2093 "Xiang-Dong Kong" @default.
- Q96123479 P2093 "Xue-Chao Zhao" @default.
- Q96123479 P2093 "Zhou-Xian Bai" @default.
- Q96123479 P31 Q13442814 @default.
- Q96123479 P356 "10.1016/J.PEDNEO.2020.04.005" @default.
- Q96123479 P577 "2020-04-15T00:00:00Z" @default.
- Q96123479 P698 "32482602" @default.
- Q96123479 P921 Q17144217 @default.