Familial and genetic association with neurodevelopmental disorders caused by a heterozygous variant in the SRRM2 gene

Familial and genetic association with neurodevelopmental disorders caused by a heterozygous variant in the SRRM2 gene

BackgroundNeurodevelopmental disorders (NDDs) are a class of disorders affecting brain development and function, characterized by an inability to reach cognitive, emotional, and motor developmental milestones. The pathology of NDDs is complex. A recent study found that variants in the SRRM2 gene cau...

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Bibliographic Details
Main Authors: Tao Zhang, Lei Xu, Hongdan Zhu, Yuyi Ying, Jinlong Ding, Haigang Ding, Xiaoliang Shi, Yao He, Xin Jin, Guiyu Xia
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-08-01
Series:Frontiers in Endocrinology
Subjects:
neurodevelopmental disorders
SRRM2 gene
whole exome sequencing
3D structure
prenatal diagnosis
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2023.1240168/full

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https://www.frontiersin.org/articles/10.3389/fendo.2023.1240168/full

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