Molecular Genetics Analysis of 70 Chinese Families With Muscular Dystrophy Using Multiplex Ligation-Dependent Probe Amplification and Next-Generation Sequencing

Background: Muscular dystrophy (MD) includes multiple types, of which dystrophinopathies caused by dystrophin (DMD) mutations are the most common types in children. An accurate identification of the causative mutation at the genomic level is critical for genetic counseling of the family, and analysi...

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Bibliographische Detailangaben
Veröffentlicht in:Front Pharmacol
Hauptverfasser: Wang, Dong, Gao, Min, Zhang, Kaihui, Jin, Ruifeng, Lv, Yuqiang, Liu, Yong, Ma, Jian, Wan, Ya, Gai, Zhongtao, Liu, Yi
Format: Artigo
Sprache:Inglês
Veröffentlicht: Frontiers Media S.A. 2019
Schlagworte:
Pharmacology
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6669794/
https://ncbi.nlm.nih.gov/pubmed/31404137
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphar.2019.00814
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