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- Q91251595 description "article scientifique publié en 2019" @default.
- Q91251595 description "artículu científicu espublizáu en xineru de 2019" @default.
- Q91251595 description "im Januar 2019 veröffentlichter wissenschaftlicher Artikel" @default.
- Q91251595 description "scientific article published on 25 January 2019" @default.
- Q91251595 description "wetenschappelijk artikel" @default.
- Q91251595 description "наукова стаття, опублікована 25 січня 2019" @default.
- Q91251595 name "Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations" @default.
- Q91251595 name "Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations" @default.
- Q91251595 type Item @default.
- Q91251595 label "Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations" @default.
- Q91251595 label "Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations" @default.
- Q91251595 prefLabel "Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations" @default.
- Q91251595 prefLabel "Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations" @default.
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- Q91251595 P304 Q91251595-94FE8A72-1A9C-45CA-B61E-549148F25CC0 @default.
- Q91251595 P31 Q91251595-D273C6C8-F63E-4DCF-8019-EB481A2F5703 @default.
- Q91251595 P356 Q91251595-CE2EDE25-4ECE-47ED-9AC6-93143E9743F3 @default.
- Q91251595 P433 Q91251595-0C2B1E16-ABD8-4E05-8FF0-9612C55FD9BD @default.
- Q91251595 P478 Q91251595-76B4B20C-AAB2-49C1-BE97-23ABBCBDBA85 @default.
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- Q91251595 P921 Q91251595-E64FE8FC-5EC7-49F5-BD1B-D63B2DA8AC71 @default.
- Q91251595 P356 J.EJMG.2019.01.014 @default.
- Q91251595 P698 30690204 @default.
- Q91251595 P1433 Q15817083 @default.
- Q91251595 P1476 "Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations" @default.
- Q91251595 P2093 "Cynthia J Curry" @default.
- Q91251595 P2093 "Erika Freitas" @default.
- Q91251595 P2093 "Fabiola P Monteiro" @default.
- Q91251595 P2093 "Fernando Kok" @default.
- Q91251595 P2093 "Jamie H Fisher" @default.
- Q91251595 P2093 "John Turocy" @default.
- Q91251595 P2093 "João Paulo Kitajima" @default.
- Q91251595 P2093 "Larissa A Costa" @default.
- Q91251595 P2093 "Robert Hevner" @default.
- Q91251595 P304 "103624" @default.
- Q91251595 P31 Q13442814 @default.
- Q91251595 P356 "10.1016/J.EJMG.2019.01.014" @default.
- Q91251595 P433 "1" @default.
- Q91251595 P478 "63" @default.
- Q91251595 P50 Q30445602 @default.
- Q91251595 P50 Q91251594 @default.
- Q91251595 P577 "2019-01-25T00:00:00Z" @default.
- Q91251595 P698 "30690204" @default.
- Q91251595 P921 Q1679678 @default.
- Q91251595 P921 Q431643 @default.