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Article

FSHD in Chinese population: characteristics of translocation and genotype-phenotype correlation.

Neurology - 10 Aug 2004

Wu Zhi-Ying, Wang Zhi-Qiang, Murong Shen-Xing, Wang Ning

Abstract excerpt

Current studies of facioscapulohumeral muscular dystrophy (FSHD) are confined to the white population. The authors surveyed 110 healthy individuals and 27 families with FSHD including 55 patients and 74 relatives by pulsed-field gel electrophoresis. The authors report the characteristics of translocation and genotype-phenotype correlation, and their results indicate 4q to 10q translocation contributes to the...

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Share to Chromosomes, Human, Pair 10
Share to Chromosomes, Human, Pair 4
Share to Deoxyribonuclease EcoRI

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Deoxyribonucleases, Type II Site-Specific

Share to Electrophoresis, Gel, Pulsed-Field

Share to Muscular Dystrophy, Facioscapulohumeral

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Share to Translocation, Genetic

Source

Identifiers

PMID: 15304602
DOI: 10.1212/01.wnl.0000133210.93075.81

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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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