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- Q92803739 description "article scientifique publié en 2019" @default.
- Q92803739 description "artículu científicu espublizáu en mayu de 2019" @default.
- Q92803739 description "scientific article published on 24 May 2019" @default.
- Q92803739 description "wetenschappelijk artikel" @default.
- Q92803739 description "наукова стаття, опублікована 24 травня 2019" @default.
- Q92803739 name "De novo variants in SETD1B cause intellectual disability, autism spectrum disorder, and epilepsy with myoclonic absences" @default.
- Q92803739 name "De novo variants in SETD1B cause intellectual disability, autism spectrum disorder, and epilepsy with myoclonic absences" @default.
- Q92803739 type Item @default.
- Q92803739 label "De novo variants in SETD1B cause intellectual disability, autism spectrum disorder, and epilepsy with myoclonic absences" @default.
- Q92803739 label "De novo variants in SETD1B cause intellectual disability, autism spectrum disorder, and epilepsy with myoclonic absences" @default.
- Q92803739 prefLabel "De novo variants in SETD1B cause intellectual disability, autism spectrum disorder, and epilepsy with myoclonic absences" @default.
- Q92803739 prefLabel "De novo variants in SETD1B cause intellectual disability, autism spectrum disorder, and epilepsy with myoclonic absences" @default.
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- Q92803739 P1476 "De novo variants in SETD1B cause intellectual disability, autism spectrum disorder, and epilepsy with myoclonic absences" @default.
- Q92803739 P2093 "Ayako Hattori" @default.
- Q92803739 P2093 "Daisuke Ieda" @default.
- Q92803739 P2093 "Hirotomo Saitsu" @default.
- Q92803739 P2093 "Ikumi Hori" @default.
- Q92803739 P2093 "Mitsuko Nakashima" @default.
- Q92803739 P2093 "Shinji Saitoh" @default.
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