Genetic Modifiers of Duchenne Muscular Dystrophy in Chinese Patients

Background: Duchenne muscular dystrophy (DMD) is a fatal, X-linked recessive muscle disorder characterized by heterogeneous progression and severity. We aimed to study the effects of single nucleotide polymorphisms (SNPs) in SPP1 and LTBP4 on DMD progression in Chinese patients. Methods: We genotype...

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Detalles Bibliográficos
Autores principales: Chen, Menglong, Wang, Liang, Li, Yaqin, Chen, Yongjun, Zhang, Huili, Zhu, Yuling, He, Ruojie, Li, Huan, Lin, Jinfu, Zhang, Yu, Zhang, Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403400/
https://www.ncbi.nlm.nih.gov/pubmed/32849198
http://dx.doi.org/10.3389/fneur.2020.00721

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403400/
https://www.ncbi.nlm.nih.gov/pubmed/32849198
http://dx.doi.org/10.3389/fneur.2020.00721

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