Work

[Analysis of clinical phenotype and gene variation of a child with neurodevelopmental disorder caused by homozygous variation of TRAPPC6B gene].

Year: 2025

Type: article

Study design: Case Report

Source: PubMed

DOI: 10.3760/cma.j.cn511374-20240918-00497

Authors: Wenxia Li, Yuke Li, Baiyun Chen, Weimeng Li, Xiaoman Zhang, Linfei Li, Qing Shang

Institutions: Zhengzhou University, Zhengzhou Children's Hospital

Language: English

Topic: Genetics and Neurodevelopmental Disorders

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W4410313338

FWCI:

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