Work

[A case of neonatal Mitochondrial DNA depletion syndrome type 13 caused by FBXL4 gene mutation].

Year: 2024

Type: article

Study design: Case Report

Source: PubMed

DOI: 10.3760/cma.j.cn511374-20240630-00360

Authors: Yuanyuan Zhu, Chenhong Wang, Junjin Chen, Xiaohong Wang, Xiaolu Ma

Institutions: Children's Hospital of Zhejiang University, Zhejiang University

Language: English

Topic: Mitochondrial Function and Pathology

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W4405250063

FWCI:

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