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Article

Becker muscular dystrophy: case report, review of the literature, and analysis of differentially expressed hub genes.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology - 1 Jan 2022

Li Min, Han Yongli, Wang Shuying, Yu Yajie, Liu Mengling, Xia Yingfeng, Weng Ze'an, Zhou Ling, He Xiaoyan, Wang Jun, He Zhi, Yu Liang, Zha Yunhong

Abstract excerpt

INTRODUCTION: Becker muscular dystrophy (BMD) is a genetic and progressive neuromuscular disease caused by mutations in the dystrophin gene with no available cure. A case report and comprehensive review of BMD cases aim to provide important clues for early diagnosis and implications for clinical practice. Genes and pathways identified from microarray data of muscle samples from patients with BMD help uncover the...

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PMID: 34731335
DOI: 10.1007/s10072-021-05499-2

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