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Article

Molecular Analysis-Based Genetic Characterization of a Cohort of Patients with Duchenne and Becker Muscular Dystrophy in Eastern China.

Chinese medical journal - 5 Apr 2018

Zhao Hui-Hui, Sun Xue-Ping, Shi Ming-Chao, Yi Yong-Xiang, Cheng Hong, Wang Xing-Xia, Xu Qing-Cheng, Ma Hong-Ming, Wu Hao-Quan, Jin Qing-Wen, Niu Qi

Abstract excerpt

BACKGROUND: Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are common X-linked recessive neuromuscular disorders caused by mutations in dystrophin gene. Multiplex polymerase chain reaction (multiplex PCR) and multiplex ligation-dependent probe amplification (MLPA) are the most common methods for detecting dystrophin gene mutations. This study aimed to contrast the two methods and discern...

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Source

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Identifiers

PMID: 29578119
DOI: 10.4103/0366-6999.228237
PMCID: PMC5887734

Genes

DMD

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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