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3. Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis

4. A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories

5. Switching From Natalizumab to Fingolimod in Multiple Sclerosis: A French Prospective Study

6. A phase II−III trial of olesoxime in subjects with amyotrophic lateral sclerosis

7. A Rare Motor Neuron Deleterious Missense Mutation in the DPYSL3 (CRMP4) Gene is Associated with ALS

8. Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis

11. Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes

15. SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations

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