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[Analysis of CX32 gene mutation and related clinical features in Chinese Han Charcot-Marie-Tooth families].

Zhonghua yi xue za zhi - 5 Jun 2012

Zhan Ya-jing, Zi Xiao-hong, Li Lin, Li Xiao-bo, Huang Shun-xiang, Li Lan, Li Xi-gui, Hu Zheng-mao, Pan Qian, Xia Kun, Tang Bei-sha, Zhang Ru-xu

Abstract excerpt

OBJECTIVE: To analyze the mutation of CX32 gene and related clinical features in Chinese Han patients with Charcot-Marie-Tooth (CMT) disease. METHODS: Thirty-four CMT families, from 2004 to 2011 at Departments of Neurology, Xiangya Hospital, Third Xiangya Hospital and National Key Laboratory of Medical Genetics, were selected for CX32 mutation screening after the exclusion of the PMP22 duplication and...

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PMID: 22944031

Genes

PMP22

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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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