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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Detalles Bibliográficos
Autores principales: Wang, Dong, Gao, Min, Zhang, Kaihui, Jin, Ruifeng, Lv, Yuqiang, Liu, Yong, Ma, Jian, Wan, Ya, Gai, Zhongtao, Liu, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Pharmacology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6669794/
https://www.ncbi.nlm.nih.gov/pubmed/31404137
http://dx.doi.org/10.3389/fphar.2019.00814

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