Yüklüyor......

Effect of genetic background on the phenotype of the Smn(2B/-) mouse model of spinal muscular atrophy

Spinal muscular atrophy (SMA) is caused by mutations or deletions in the Survival Motor Neuron 1 (SMN1) gene in humans. Modifiers of the SMA symptoms have been identified and genetic background has a substantial effect in the phenotype and survival of the severe mouse model of SMA. Previously, we ge...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Hum Mol Genet
Asıl Yazarlar: Eshraghi, Mehdi, McFall, Emily, Gibeault, Sabrina, Kothary, Rashmi
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2016
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5409218/
https://ncbi.nlm.nih.gov/pubmed/28172892
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw278
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!