期刊
TRENDS IN GENETICS
卷 36, 期 4, 页码 228-231出版社
CELL PRESS
DOI: 10.1016/j.tig.2020.01.005
关键词
-
资金
- Australian National Medical and Health Research Council (NHMRC) [1063960, 1066177, 1037196]
- 'Ramon y Cajal' fellowship from the Spanish MINECO [RyC2018-024106-I]
It is still unclear how genetic factors of autism spectrum disorder (ASD) are implicated in the significant clinical heterogeneity ranging from intellectual disability (ID) to highfunctioning profiles. Here, evidence from recent genetic studies encompassing common and rare variants are combined to suggest a genetic model that may explain the broad gradient of phenotypic severity observed in ASD.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据