Article

Identification of a de novo mutation of FOXG1gene and comprehensive analysis for molecular factors in Chinese FOXG1-related Rett syndrome

2022-08-26

Abstract excerpt

<title>Abstract</title><p>Currently, majority of the FOXG1-related Rett syndrome have been identified in Europeans and North Americans, and relatively few Chinese cases were reported. We identified a<italic>de novo</italic>nonsense mutation of<italic>FOXG1</italic>in a female child with Rett syndrome out of 73 Chinese children with neurodevelopmental disorders in our cohort. In order to have a comprehensive view o...

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Literature Corpus work: e2c77609-fa99-5ee4-b656-304d1617fa42
DOI: 10.21203/rs.3.rs-1953777/v1

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