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- Q90783511 description "article scientifique publié en 2018" @default.
- Q90783511 description "artículu científicu espublizáu n'avientu de 2018" @default.
- Q90783511 description "im Dezember 2018 veröffentlichter wissenschaftlicher Artikel" @default.
- Q90783511 description "scientific article published on 24 December 2018" @default.
- Q90783511 description "wetenschappelijk artikel" @default.
- Q90783511 description "наукова стаття, опублікована в грудні 2018" @default.
- Q90783511 name "A trafficking-deficient KCNQ1 mutation, T587M, causes a severe phenotype of long QT syndrome by interfering with intracellular hERG transport" @default.
- Q90783511 name "A trafficking-deficient KCNQ1 mutation, T587M, causes a severe phenotype of long QT syndrome by interfering with intracellular hERG transport" @default.
- Q90783511 type Item @default.
- Q90783511 label "A trafficking-deficient KCNQ1 mutation, T587M, causes a severe phenotype of long QT syndrome by interfering with intracellular hERG transport" @default.
- Q90783511 label "A trafficking-deficient KCNQ1 mutation, T587M, causes a severe phenotype of long QT syndrome by interfering with intracellular hERG transport" @default.
- Q90783511 prefLabel "A trafficking-deficient KCNQ1 mutation, T587M, causes a severe phenotype of long QT syndrome by interfering with intracellular hERG transport" @default.
- Q90783511 prefLabel "A trafficking-deficient KCNQ1 mutation, T587M, causes a severe phenotype of long QT syndrome by interfering with intracellular hERG transport" @default.
- Q90783511 P1433 Q90783511-ABFE9A6E-4AD9-4B4C-8EE4-A920D6DAF889 @default.
- Q90783511 P1476 Q90783511-3ADC101B-3529-45C5-859D-36B4FEA5A0EF @default.
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- Q90783511 P2093 Q90783511-B97AE5A1-086D-4773-B414-024D60C0D3B6 @default.
- Q90783511 P2093 Q90783511-CCBFB37E-315B-44E1-A25F-1DF6FBFEBFC8 @default.
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- Q90783511 P304 Q90783511-DB1E01F7-895D-4440-8AFF-4F63072A3D3E @default.
- Q90783511 P31 Q90783511-DB80129C-3B85-4008-99CC-1A70F5C63190 @default.
- Q90783511 P356 Q90783511-B1724098-5881-4BD2-A8FA-BF262984F32C @default.
- Q90783511 P433 Q90783511-0509C721-D9F4-4D09-BAE9-683F99DA24DA @default.
- Q90783511 P478 Q90783511-2B99BA1E-F90F-4A52-B7F1-C26457E54487 @default.
- Q90783511 P577 Q90783511-CC5F353E-FB2E-40C3-946C-4038FEE8A01E @default.
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- Q90783511 P921 Q90783511-CA9D0884-689E-47AF-8157-F45974E8C71C @default.
- Q90783511 P356 J.JJCC.2018.10.011 @default.
- Q90783511 P698 30591322 @default.
- Q90783511 P1433 Q15816342 @default.
- Q90783511 P1476 "A trafficking-deficient KCNQ1 mutation, T587M, causes a severe phenotype of long QT syndrome by interfering with intracellular hERG transport" @default.
- Q90783511 P2093 "Futoshi Toyoda" @default.
- Q90783511 P2093 "Hiroshi Matsuura" @default.
- Q90783511 P2093 "Jie Wu" @default.
- Q90783511 P2093 "Keiko Tsuji" @default.
- Q90783511 P2093 "Kotoe Takenaka" @default.
- Q90783511 P2093 "Minoru Horie" @default.
- Q90783511 P2093 "Tomoko Sakaguchi" @default.
- Q90783511 P304 "343-350" @default.
- Q90783511 P31 Q13442814 @default.
- Q90783511 P356 "10.1016/J.JJCC.2018.10.011" @default.
- Q90783511 P433 "5" @default.
- Q90783511 P478 "73" @default.
- Q90783511 P577 "2018-12-24T00:00:00Z" @default.
- Q90783511 P698 "30591322" @default.
- Q90783511 P921 Q653924 @default.