Načítá se...
Mechanism of Splicing Regulation of Spinal Muscular Atrophy Genes
Spinal muscular atrophy (SMA) is one of the major genetic disorders associated with infant mortality. More than 90% cases of SMA result from deletions or mutations of Survival Motor Neuron 1 (SMN1) gene. SMN2, a nearly identical copy of SMN1, does not compensate for the loss of SMN1 due to predomina...
Uloženo v:
| Vydáno v: | Adv Neurobiol |
|---|---|
| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2018
|
| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6026014/ https://ncbi.nlm.nih.gov/pubmed/29916015 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-3-319-89689-2_2 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|