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Inhibition of FLT1 ameliorates muscular dystrophy phenotype by increased vasculature in a mouse model of Duchenne muscular dystrophy
Verma, Mayank, Shimizu-Motohashi, Yuko, Asakura, Yoko, Ennen, James P., Bosco, Jennifer, Zhou, Zhiwei, Fong, Guo-Hua, Josiah, Serene, Keefe, Dennis, Asakura, Atsushi, Cox, Gregory A.Volume:
15
Language:
english
Journal:
PLOS Genetics
DOI:
10.1371/journal.pgen.1008468
Date:
December, 2019
File:
PDF, 4.16 MB
english, 2019