Increasing LRP4 diminishes neuromuscular deficits in a mouse model of Duchenne muscular dystrophy

Duchenne muscular dystrophy (DMD) is an X-linked neuromuscular disease characterized by progressive wasting of skeletal muscles. The neuromuscular junction (NMJ) is a synapse between motor neurons and skeletal muscle fibers, critical for the control of muscle contraction. The NMJ decline is observed...

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Detalles Bibliográficos
Autores principales: Hui, Tiankun, Jing, Hongyang, Zhou, Tian, Chen, Peng, Liu, Ziyang, Dong, Xia, Yan, Min, Ren, Dongyan, Zou, Suqi, Wang, Shunqi, Fei, Erkang, Hong, Daojun, Lai, Xinsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
General Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8369839/
https://www.ncbi.nlm.nih.gov/pubmed/33987657
http://dx.doi.org/10.1093/hmg/ddab135

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8369839/
https://www.ncbi.nlm.nih.gov/pubmed/33987657
http://dx.doi.org/10.1093/hmg/ddab135

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