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Article

Coexistence of peripheral myelin protein 22 and dystrophin mutations in a chinese boy.

Muscle & nerve - 1 Dec 2013

Wang Zhanjun, Cui Fang, Chen Dajun, Pu Chuanqiang, Chen Zhaohui, Yang Fei, Wu Honghu, Huang Xusheng

Abstract excerpt

INTRODUCTION: We describe a 10-year-old Chinese boy with features of Charcot-Marie-Tooth disease (CMT) and Duchenne muscular dystrophy (DMD). METHODS: Case report. RESULTS: Weakness and mild sensory loss in the distal extremities, pes cavus, and nerve conduction findings suggested demyelinating n...

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Source

Identifiers

PMID: 23740413
DOI: 10.1002/mus.23918

Genes

DMD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23740413-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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