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- Q73131079 description "artículu científicu espublizáu n'ochobre de 2000" @default.
- Q73131079 description "im Oktober 2000 veröffentlichter wissenschaftlicher Artikel" @default.
- Q73131079 description "scientific article published on 01 October 2000" @default.
- Q73131079 description "wetenschappelijk artikel" @default.
- Q73131079 description "наукова стаття, опублікована в жовтні 2000" @default.
- Q73131079 name "A novel deletion mutation within the carboxyl terminus of the copper-transporting ATPase gene causes Wilson disease" @default.
- Q73131079 name "A novel deletion mutation within the carboxyl terminus of the copper-transporting ATPase gene causes Wilson disease" @default.
- Q73131079 type Item @default.
- Q73131079 label "A novel deletion mutation within the carboxyl terminus of the copper-transporting ATPase gene causes Wilson disease" @default.
- Q73131079 label "A novel deletion mutation within the carboxyl terminus of the copper-transporting ATPase gene causes Wilson disease" @default.
- Q73131079 prefLabel "A novel deletion mutation within the carboxyl terminus of the copper-transporting ATPase gene causes Wilson disease" @default.
- Q73131079 prefLabel "A novel deletion mutation within the carboxyl terminus of the copper-transporting ATPase gene causes Wilson disease" @default.
- Q73131079 P1433 Q73131079-0AFD85E1-9453-489D-B764-17D860095B83 @default.
- Q73131079 P1476 Q73131079-4B7B5C94-1D58-4B53-9335-E4DAAD367CE3 @default.
- Q73131079 P2093 Q73131079-1EDA5AD8-8C82-4206-AF40-5D212096EF4E @default.
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- Q73131079 P2093 Q73131079-98486A56-9B78-490F-A9C6-6F00131092D7 @default.
- Q73131079 P2093 Q73131079-9F8C2E23-96CD-40C0-B855-8364D95E1811 @default.
- Q73131079 P2093 Q73131079-A0384CFD-AE66-42ED-B4C6-912FEA10F132 @default.
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- Q73131079 P2093 Q73131079-C8780C15-0743-40CA-81AF-0DEB39724055 @default.
- Q73131079 P2860 Q73131079-28E3FB12-8CE0-4AA1-9618-2AB622739BED @default.
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- Q73131079 P304 Q73131079-ACEF16F5-898A-425A-9090-B80E34ACAC2B @default.
- Q73131079 P31 Q73131079-38E0C332-23DF-4A60-B2FA-D1A2DE427CF9 @default.
- Q73131079 P356 Q73131079-BBDACFB0-2AEA-41BD-AE0B-6623B95BC7D2 @default.
- Q73131079 P433 Q73131079-1C9FC39A-953D-4958-859E-19CB029B79CB @default.
- Q73131079 P478 Q73131079-DCB191AB-C156-4260-8572-046F1D769BA8 @default.
- Q73131079 P577 Q73131079-126698FE-452E-489C-91E3-8F6CCBD2E65A @default.
- Q73131079 P698 Q73131079-A9E9D635-DBC2-46D6-AC28-8D67ABA37E4E @default.
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- Q73131079 P356 S0022-510X(00)00399-3 @default.
- Q73131079 P698 11054498 @default.
- Q73131079 P1433 Q6296168 @default.
- Q73131079 P1476 "A novel deletion mutation within the carboxyl terminus of the copper-transporting ATPase gene causes Wilson disease" @default.
- Q73131079 P2093 "A Al Zaben" @default.
- Q73131079 P2093 "A Awada" @default.
- Q73131079 P2093 "I Al Traif" @default.
- Q73131079 P2093 "M Al Jumah" @default.
- Q73131079 P2093 "M Fraser" @default.
- Q73131079 P2093 "M Paterson" @default.
- Q73131079 P2093 "R Majumdar" @default.
- Q73131079 P2093 "S Al Rajeh" @default.
- Q73131079 P2860 Q22008012 @default.
- Q73131079 P2860 Q24336948 @default.
- Q73131079 P2860 Q33682273 @default.
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- Q73131079 P2860 Q48075338 @default.
- Q73131079 P2860 Q74048061 @default.
- Q73131079 P2860 Q74310623 @default.
- Q73131079 P304 "140-143" @default.
- Q73131079 P31 Q13442814 @default.
- Q73131079 P356 "10.1016/S0022-510X(00)00399-3" @default.
- Q73131079 P433 "S 1-2" @default.
- Q73131079 P478 "179" @default.
- Q73131079 P577 "2000-10-01T00:00:00Z" @default.
- Q73131079 P698 "11054498" @default.
- Q73131079 P921 Q117121 @default.