Código QR (código de barras bidimensional)

Co-occurrence of rare variants implicates gene pairs in cytoskeletal pathways and is associated with increased severity in autism spectrum disorder

Abstract Background The genetic basis of autism spectrum disorder (ASD) is complicated by high heritability and substantial heterogeneity, in which de novo variants and polygenic burden from common variants have not been comprehensively elucidated. Increasing evidence indicates that aggregates of ra...

Fuld beskrivelse

Na minha lista:
Principais autores: Hyeji Lee, Kahee Ko, Seoyeon Kim, Ganghee Lee, Soowhee Kim, Jihae Lee, Da-Yea Song, Guiyoung Bong, Jae Hyun Han, Jeewon Lee, Ye Rim Kim, Yoojeong Lee, Eunjoon Kim, Anders D. Børglum, Jakob Grove, So Hyun Kim, Woong Sun, Hee Jeong Yoo, Joon-Yong An
Format: Artigo
Sprog:Inglês
Udgivet: BMC 2026-03-01
Serier:Genome Biology
Fag:
Whole-genome sequencing
Whole-exome sequencing
ASD
Rare variants
Gene combinations
Cytoskeleton pathway
Online adgang:https://doi.org/10.1186/s13059-026-04041-x
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker