Utrophin Compensates dystrophin Loss during Mouse Spermatogenesis

Abstract Duchenne muscular dystrophy (DMD) is an X-linked genetic disorder resulting from mutations in the dystrophin gene. The mdx/utrn −/− mouse, lacking in both dystrophin and its autosomal homologue utrophin, is commonly used to model the clinical symptoms of DMD. Interestingly, these mice are i...

Fuld beskrivelse

Bibliografiske detaljer

Principais autores:	Hung-Chih Chen, Yu-Feng Chin, David J. Lundy, Chung-Tiang Liang, Ya-Hui Chi, Paolin Kuo, Patrick C. H. Hsieh
Format:	Artigo
Sprog:	Inglês
Udgivet:	Nature Portfolio 2017-08-01
Serier:	Scientific Reports
Online adgang:	https://doi.org/10.1038/s41598-017-05993-8
Tags:	Tilføj Tag Ingen Tags, Vær først til at tagge denne postø!