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Article

[Peroneal myoatrophy type 4H FGD4 new gene mutation in one case and literature review].

Zhonghua er ke za zhi = Chinese journal of pediatrics - 1 Mar 2016

Yan Chen, Yuan Zhefeng, Xu Lu, Jiang Lihua, Gao Feng

Abstract excerpt

OBJECTIVE: To explore the clinical and gene mutation characteristics of children with peroneal myoatrophy FGD4 mutations. METHOD: The clinical data of a patient with peroneal myoatrophy with novel FGD4 gene mutations were collected, the related literature was searched from China National Knowledge Infrastructure, Wanfang Data Knowledge Service Platform, National Center for Biotechnology Information and PubMed (up...

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Source

Identifiers

PMID: 26957070
DOI: 10.3760/cma.j.issn.0578-1310.2016.03.013

Genes

FGD4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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