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- Q96159216 description "article scientifique publié en 2020" @default.
- Q96159216 description "artículu científicu espublizáu en xunu de 2020" @default.
- Q96159216 description "im Juni 2020 veröffentlichter wissenschaftlicher Artikel" @default.
- Q96159216 description "scientific article published on 04 June 2020" @default.
- Q96159216 description "wetenschappelijk artikel" @default.
- Q96159216 description "наукова стаття, опублікована 4 червня 2020" @default.
- Q96159216 name "A 24-base pair deletion in the ABO gene causes a hereditary splice site defect: a novel mechanism underlying ABO blood group O" @default.
- Q96159216 name "A 24-base pair deletion in the ABO gene causes a hereditary splice site defect: a novel mechanism underlying ABO blood group O" @default.
- Q96159216 type Item @default.
- Q96159216 label "A 24-base pair deletion in the ABO gene causes a hereditary splice site defect: a novel mechanism underlying ABO blood group O" @default.
- Q96159216 label "A 24-base pair deletion in the ABO gene causes a hereditary splice site defect: a novel mechanism underlying ABO blood group O" @default.
- Q96159216 prefLabel "A 24-base pair deletion in the ABO gene causes a hereditary splice site defect: a novel mechanism underlying ABO blood group O" @default.
- Q96159216 prefLabel "A 24-base pair deletion in the ABO gene causes a hereditary splice site defect: a novel mechanism underlying ABO blood group O" @default.
- Q96159216 P1433 Q96159216-24E69B2E-0DEC-4183-80D2-3C9B4281FB6C @default.
- Q96159216 P1476 Q96159216-8F349DA9-6895-4AB7-8929-2DA19262580B @default.
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- Q96159216 P2093 Q96159216-2F9733C3-1D0F-4BF0-9686-FC9E89D4BCDB @default.
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- Q96159216 P2093 Q96159216-959221D0-544B-4662-83C3-A19344087204 @default.
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- Q96159216 P31 Q96159216-4BAB6DB5-7B17-485A-B54F-0B384E3F2BF3 @default.
- Q96159216 P356 Q96159216-C1429E1E-ADB7-4533-99F2-32DE04DFE993 @default.
- Q96159216 P50 Q96159216-1B065CB6-4DD9-4C07-9462-7D4AE22CD262 @default.
- Q96159216 P577 Q96159216-B91573DE-58A5-43B8-A276-818A3D5BB525 @default.
- Q96159216 P698 Q96159216-CF003E09-538E-4579-B884-6F07E53BA4FE @default.
- Q96159216 P932 Q96159216-643235E7-8148-46B7-9A18-46520DACB6D2 @default.
- Q96159216 P356 TRF.15907 @default.
- Q96159216 P698 32500601 @default.
- Q96159216 P1433 Q15758500 @default.
- Q96159216 P1476 "A 24-base pair deletion in the ABO gene causes a hereditary splice site defect: a novel mechanism underlying ABO blood group O" @default.
- Q96159216 P2093 "Andrea Wagner" @default.
- Q96159216 P2093 "Ariane Pessentheiner" @default.
- Q96159216 P2093 "Camilla Drexler" @default.
- Q96159216 P2093 "Claudia Bernecker" @default.
- Q96159216 P2093 "Juliane Gertrude Bogner-Strauß" @default.
- Q96159216 P2093 "Thomas Wagner" @default.
- Q96159216 P2093 "Wolfgang Helmberg" @default.
- Q96159216 P31 Q13442814 @default.
- Q96159216 P356 "10.1111/TRF.15907" @default.
- Q96159216 P50 Q92116141 @default.
- Q96159216 P577 "2020-06-04T00:00:00Z" @default.
- Q96159216 P698 "32500601" @default.
- Q96159216 P932 "7496400" @default.