Načítá se...
A low absolute number of expanded transcripts is involved in myotonic dystrophy type 1 manifestation in muscle
Muscular manifestation of myotonic dystrophy type 1 (DM1), a common inheritable degenerative multisystem disorder, is mainly caused by expression of RNA from a (CTG·CAG)(n)-expanded DM1 locus. Here, we report on comparative profiling of expression of normal and expanded endogenous or transgenic tran...
Uloženo v:
| Vydáno v: | Hum Mol Genet |
|---|---|
| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2016
|
| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4805313/ https://ncbi.nlm.nih.gov/pubmed/26908607 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw042 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|