Work

[Analysis of SMARCA2 gene mutation in a child with Nicolaides-Baraitser syndrome].

Year: 2019

Type: article

Study design: Case Report

Source: PubMed

DOI: 10.3760/cma.j.issn.1003-9406.2019.12.009

Authors: Xuyun Hu, Ruolan Guo, Jun Guo, Wei Li, Li Liu, Chanjuan Hao

Institutions: Capital Medical University, Beijing Children’s Hospital

Language: English

Topic: Genomics and Rare Diseases

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W3007603594

FWCI: 0.135

Cites:

Cited by: 1

Related to: 10