Functional characterization of SMN evolution in mouse models of SMA

Spinal Muscular Atrophy (SMA) is a monogenic neurodegenerative disorder and the leading genetic cause of infantile mortality. While several functions have been ascribed to the SMN (survival motor neuron) protein, their specific contribution to the disease has yet to be fully elucidated. We hypothesi...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Sci Rep
Hlavní autoři: Osman, Erkan Y., Bolding, Madeline R., Villalón, Eric, Kaifer, Kevin A., Lorson, Zachary C., Tisdale, Sarah, Hao, Yue, Conant, Gavin C., Pires, J. Chris, Pellizzoni, Livio, Lorson, Christian L.
Médium: Artigo
Jazyk:Inglês
Vydáno: Nature Publishing Group UK 2019
Témata:
Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6603021/
https://ncbi.nlm.nih.gov/pubmed/31263170
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-45822-8
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky