<i>SMN1</i> gene, but not <i>SMN2</i> , is a risk factor for sporadic ALS
P. Corcia(Inserm), Christian Andrés(Inserm), William Camu, Catherine Antar(Université de Tours), Jean‐Michel Halimi(Centre Hospitalier Universitaire de Tours), Patrick Vourc’h(Université de Tours), Bertrand de Toffol(Université de Tours), Bruno Giraudeau(Inserm), Sylviane Védrine(Université de Tours)
Cited by 88
Related Papers
Association Between Administration of Systemic Corticosteroids and Mortality Among Critically Ill Patients With COVID-19
|JAMA|2020|2.4k
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
|Nature Genetics|2008|1.5k
X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family
|The American Journal of Human Genetics|2004|762
Enteral versus parenteral early nutrition in ventilated adults with shock: a randomised, controlled, multicentre, open-label, parallel-group study (NUTRIREA-2)
|The Lancet|2017|568
Dyslipidemia is a protective factor in amyotrophic lateral sclerosis
|Neurology|2008|543