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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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Principais autores: Brkušanin Miloš, Jeftović-Velkova Irena, Jovanović Vladimir M., Perić Stojan, Pešović Jovan, Brajušković Goran, Stević Zorica, Savić-Pavićević Dušanka
Format: Artigo
Sprog:Inglês
Udgivet: Serbian Medical Society 2018-01-01
Serier:Srpski Arhiv za Celokupno Lekarstvo
Fag:
survival motor neuron
amyotrophic lateral sclerosis
H4F5
NAIP
SMN1
Online adgang:http://www.doiserbia.nb.rs/img/doi/0370-8179/2018/0370-81791800069B.pdf
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