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Genetic dissection identifies Necdin as a driver gene in a mouse model of paternal 15q duplications
oleh: Kota Tamada, Keita Fukumoto, Tsuyoshi Toya, Nobuhiro Nakai, Janak R. Awasthi, Shinji Tanaka, Shigeo Okabe, François Spitz, Fumihito Saitow, Hidenori Suzuki, Toru Takumi
Format: | Article |
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Diterbitkan: | Nature Portfolio 2021-07-01 |
Deskripsi
Duplication of chromosome 15q11-q13 is associated with autism spectrum disorder (ASD). Here, the authors show that in mice paternal Dup15q results in ASD-like neuronal and behavioural impairment driven by Necdin.