Mutations affecting the N-terminal domains of SHANK3 point to different pathomechanisms in neurodevelopmental disorders.

Woike, Daniel; Wang, Emily; Tibbe, Debora; Hassani Nia, Fatemeh; Failla, Antonio Virgilio; Kibæk, Maria; Overgård, Tinett Martesen; Larsen, Martin J; Fagerberg, Christina R; Barsukov, Igor; Kreienkamp, Hans-Jürgen

Woike, Daniel; Wang, Emily; Tibbe, Debora; Hassani Nia, Fatemeh; Failla, Antonio Virgilio; Kibæk, Maria; Overgård, Tinett Martesen; Larsen, Martin J; Fagerberg, Christina R; Barsukov, Igor; Kreienkamp, Hans-Jürgen.

Afiliação

Woike D; Institute for Human Genetics, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Wang E; Institute of Integrative Biology, University of Liverpool, Liverpool, UK.
Tibbe D; Institute for Human Genetics, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Hassani Nia F; Institute for Human Genetics, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Failla AV; UKE Microscopic Imaging Facility (UMIF), University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Kibæk M; H C Andersen Children's Hospital, Odense University Hospital, Odense, Denmark.
Overgård TM; Department of Psychiatry, Middelfart, Region of Southern Denmark, Denmark.
Larsen MJ; H C Andersen Children's Hospital, Odense University Hospital, Odense, Denmark.
Fagerberg CR; Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.
Barsukov I; H C Andersen Children's Hospital, Odense University Hospital, Odense, Denmark.
Kreienkamp HJ; Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.

Sci Rep ; 12(1): 902, 2022 01 18.

Article em En | MEDLINE | ID: mdl-35042901

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sinapses Idioma: En Revista: Sci Rep Ano de publicação: 2022 Tipo de documento: Article

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