Zobrazeno 1 - 4
of 4
pro vyhledávání: '"C. Aaron Larsen"'
Autor:
Kevin M. Flanigan, C. Aaron Larsen, Robert B. Weiss, Carsten B. Bönnemann, Diane M. Dunn, Livija Medne
Publikováno v:
Muscle & Nerve. 44:822-825
The use of hybridization-based methods for DMD mutation analysis is increasingly common. We report a case of Becker Muscular Dystrophy in which discrepant results between a PCR-based (SCAIP) and a comparative genomic hybridization assay incompletely
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb56a90629162dd15c6d45f07d09a35c
https://doi.org/10.1002/mus.22226
https://doi.org/10.1002/mus.22226
Autor:
Michael T. Howard, C. Aaron Larsen
Duchenne muscular dystrophy (DMD), a severe muscle-wasting disease, is caused by mutations in the DMD gene, which encodes for the protein dystrophin. Its regulation is of therapeutic interest as even small changes in expression of functional dystroph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92df42d557a77943d2ac37a58bf8228d
https://europepmc.org/articles/PMC4114305/
https://europepmc.org/articles/PMC4114305/
Autor:
Peter P. Nghiem, David A. Detwiler, Zheng Fan, Jiahui Wang, Kevin M. Flanigan, Daniel J. Bogan, Eric P. Hoffman, Scott J. Schatzberg, Sandra P. Tou, Robert W. Grange, Ratna Bhavaraju-Sanka, Martin K. Childers, Joe N. Kornegay, Xiao Xiao, Bruce P. Keene, James F. Howard, Juan Li, C. Aaron Larsen, Janet R. Bogan, Martin Styner
Duchenne muscular dystrophy (DMD) is an X-linked recessive disorder in which the loss of dystrophin causes progressive degeneration of skeletal and cardiac muscle. Potential therapies that carry substantial risk, such as gene and cell-based approache
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08786c7ab7577718d12cf4e983ab8abd
https://europepmc.org/articles/PMC3911884/
https://europepmc.org/articles/PMC3911884/
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