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...

Full beskrivning

Sparad:
Bibliografiska uppgifter
I publikationen:Front Neurol
Huvudupphovsmän: Chen, Menglong, Wang, Liang, Li, Yaqin, Chen, Yongjun, Zhang, Huili, Zhu, Yuling, He, Ruojie, Li, Huan, Lin, Jinfu, Zhang, Yu, Zhang, Cheng
Materialtyp: Artigo
Språk:Inglês
Publicerad: Frontiers Media S.A. 2020
Ämnen:
Neurology
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC7403400/
https://ncbi.nlm.nih.gov/pubmed/32849198
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2020.00721
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!

Liknande verk