Copies of the survival motor neuron gene in spinal muscular atrophy: the more, the better
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
Reference12 articles.
1. A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing;Pellizoni;Cell,1998
2. Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos;Schrank;Proc Natl Acad Sci USA,1997
3. SMN mutants of spinal muscular atrophy patients are defective in binding to snRNP proteins;Pellizoni;Proc Natl Acad Sci USA,1999
4. Correlation between severity and SMN protein level in spinal muscular atrophy;Lefebvre;Nat Genet,1997
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1. Joint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patients;Journal of Human Genetics;2015-08-27
2. Synaptic defects in type I spinal muscular atrophy in human development;The Journal of Pathology;2012-12-17
3. Treatment strategies for spinal muscular atrophy;Translational Neuroscience;2010-01-01
4. Survival motor neuron gene 2 silencing by DNA methylation correlates with spinal muscular atrophy disease severity and can be bypassed by histone deacetylase inhibition;Human Molecular Genetics;2008-10-29
5. Drug discovery for spinal muscular atrophy;Expert Opinion on Drug Discovery;2007-04
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