Protein-truncating variants and deletions of SHANK2 are associated with autism spectrum disorder and other neurodevelopmental concerns

Abstract Background SHANK2 disorder is a rare neurodevelopmental disorder caused by a deletion or pathogenic sequence variant of the SHANK2 gene and is associated with autism spectrum disorder (ASD), intellectual disability (ID), and developmental delay. To date, research in SHANK2 has focused on la...

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Λεπτομέρειες βιβλιογραφικής εγγραφής

Κύριοι συγγραφείς:	Hailey Silver, Rori Greenberg, Paige M. Siper, Jessica Zweifach, Renee Soufer, Mustafa Sahin, Elizabeth Berry-Kravis, Latha Valluripalli Soorya, Audrey Thurm, Jonathan A. Bernstein, Alexander Kolevzon, Dorothy E. Grice, Joseph D. Buxbaum, Tess Levy
Μορφή:	Artigo
Γλώσσα:	Inglês
Έκδοση:	BMC 2025-04-01
Σειρά:	Journal of Neurodevelopmental Disorders
Θέματα:	SHANK2 Autism spectrum disorder Developmental delay Intellectual and developmental disability Phenotype
Διαθέσιμο Online:	https://doi.org/10.1186/s11689-025-09600-0
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