Shared rare genetic variants in multiplex autism families suggest a social memory gene under selection

Shared rare genetic variants in multiplex autism families suggest a social memory gene under selection

Abstract Autism spectrum disorder (ASD) affects up to 1 in 59 children, and is one of the most common neurodevelopmental disorders. Recent genomic studies have highlighted the role of rare variants in ASD. This study aimed to identify genes affected by rare variants shared by siblings with ASD and v...

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Bibliographic Details
Main Authors: Kang Seon Lee, Taeyeop Lee, Mujun Kim, Elizaveta Ignatova, Hyo-Jeong Ban, Min Kyung Sung, Younghoon Kim, Youn-Jae Kim, Jin-Hee Han, Jung Kyoon Choi
Format: Article
Language:English
Published: Nature Portfolio 2025-01-01
Series:Scientific Reports
Subjects:
Autism spectrum disorder
Shared rare variant
Social novelty
Social memory
FRRS1L
AMPA receptor
Online Access:https://doi.org/10.1038/s41598-024-83839-w
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https://doi.org/10.1038/s41598-024-83839-w

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