Omigapil Treatment Decreases Fibrosis and Improves Respiratory Rate in dy2J Mouse Model of Congenital Muscular Dystrophy-Reference-Cited by-同舟云学术

Omigapil Treatment Decreases Fibrosis and Improves Respiratory Rate in dy2J Mouse Model of Congenital Muscular Dystrophy

Published:2013-06-06 Issue:6 Volume:8 Page:e65468
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Yu Qing,Sali Arpana,Van der Meulen Jack,Creeden Brittany K.,Gordish-Dressman Heather,Rutkowski Anne,Rayavarapu Sree,Uaesoontrachoon Kitipong,Huynh Tony,Nagaraju Kanneboyina,Spurney Christopher F.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

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3. The congenital muscular dystrophies in 2004: a century of exciting progress;F Muntoni;Neuromuscul Disord,2004

4. Massive muscle cell degeneration in the early stage of merosin-deficient congenital muscular dystrophy;YK Hayashi;Neuromuscul Disord,2001

5. Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models;W Kuang;J Clin Invest,1998

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