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Article

[Zellweger syndrome caused by PEX6 gene variation in 2 cases and literature review].

Zhonghua er ke za zhi = Chinese journal of pediatrics - 2 Jan 2024

Yang P, Zeng C Z, Tao X W, Rong S W, Long Y, Zeng L K

Abstract excerpt

Objective: To summarize the clinical features and genetic characteristics of Zellweger spectrum disorder caused by PEX6 gene variation. Methods: This was a case series research. Clinical date and genetic results of 2 neonatal cases of Zellweger syndrome caused by PEX6 gene variation in Wuhan Children's Hospital, Tongji Medical College, Huazhong University of Science & Technology and Affiliated Hospital of...

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Identifiers

PMID: 38154976
DOI: 10.3760/cma.j.cn112140-20230914-00191

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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