Aberrant myokine signaling in congenital myotonic dystrophy

Myotonic dystrophy types 1 (DM1) and 2 (DM2) are dominantly-inherited neuromuscular disorders caused by a toxic gain-of-function of expanded CUG and CCUG repeats, respectively. Although both disorders are clinically similar, congenital myotonic dystrophy (CDM), a severe DM form, is only found in DM1...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Cell Rep
Päätekijät: Nakamori, Masayuki, Hamanaka, Kohei, Thomas, James D., Wang, Eric T., Hayashi, Yukiko K., Takahashi, Masanori P., Swanson, Maurice S., Nishino, Ichizo, Mochizuki, Hideki
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2017
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5689469/
https://ncbi.nlm.nih.gov/pubmed/29091763
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.celrep.2017.10.018
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