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pro vyhledávání: '"Crystal Faelan"'
Autor:
Johannes Dworzak, Daniel G. Rudmann, Famke Aeffner, Kristin Wilson, Crystal Faelan, Suzanne Kanaly, Manish Ranjitkar, Holger Lange, J Kris Piper, Steven A. Moore, Joshua C. Black, Anthony J. Milici, D. Frank, Jay S. Charleston, G. David Young, Alexander Moody
Publikováno v:
Archives of Pathology & Laboratory Medicine. 143:197-205
Context.—Duchenne muscular dystrophy is a rare, progressive, and fatal neuromuscular disease caused by dystrophin protein loss. Common investigational treatment approaches aim at increasing dystrophin expression in diseased muscle. Some clinical tr
Autor:
Jay S. Charleston, G. David Young, Kristin Wilson, Daniel G. Rudmann, Jon Tinsley, Crystal Faelan, Steven A. Moore, Anthony J. Milici, D. Frank, Janet C. Patterson-Kane
Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are neuromuscular disorders that primarily affect boys due to an X-linked mutation in the DMD gene, resulting in reduced to near absence of dystrophin or expression of truncated fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdd011661252ff27fbe18cfc203f5f1e
https://europepmc.org/articles/PMC5788182/
https://europepmc.org/articles/PMC5788182/