SMN1 copy number as a modifying factor of survival in Serbian patients with sporadic amyotrophic lateral sclerosis

Introduction/Objective. Amyotrophic lateral sclerosis (ALS) is a devastating motor neuron disease. The majority of cases are apparently sporadic ALS (SALS) with variants in susceptibility genes or sometimes in high-risk ALS genes. Two ALS susceptibility genes are SMN1, whose functional loss causes s...

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Prif Awduron:	Brkušanin Miloš, Jeftović-Velkova Irena, Jovanović Vladimir M., Perić Stojan, Pešović Jovan, Brajušković Goran, Stević Zorica, Savić-Pavićević Dušanka
Fformat:	Artigo
Iaith:	Inglês
Cyhoeddwyd:	Serbian Medical Society 2018-01-01
Cyfres:	Srpski Arhiv za Celokupno Lekarstvo
Pynciau:	survival motor neuron amyotrophic lateral sclerosis H4F5 NAIP SMN1
Mynediad Ar-lein:	http://www.doiserbia.nb.rs/img/doi/0370-8179/2018/0370-81791800069B.pdf
Tagiau:	Ychwanegu Tag Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!