| Literature DB >> 26454198 |
Xuan Guan1, Melissa A Goddard1, David L Mack2, Martin K Childers3.
Abstract
Current treatment options for patients with monogenetic congenital myopathies (MCM) ameliorate the symptoms of the disorder without resolving the underlying cause. However, gene therapies are being developed where the mutated or deficient gene target is replaced. Preclinical findings in animal models appear promising, as illustrated by gene replacement for X-linked myotubular myopathy (XLMTM) in canine and murine models. Prospective applications and approaches to gene replacement therapy, using these disorders as examples, are discussed in this review.Entities:
Keywords: Animal models; Gene therapy; Muscle disease; Muscular dystrophy; Myopathy
Mesh:
Substances:
Year: 2015 PMID: 26454198 PMCID: PMC4826856 DOI: 10.1016/j.ymeth.2015.10.004
Source DB: PubMed Journal: Methods ISSN: 1046-2023 Impact factor: 3.608