5 results on '"Cazeneuve, Cécile"'
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2. SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations
3. Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia
4. Cystic fibrosis patients with the 3272-26A>G splicing mutation have milder disease than F508del homozygotes: a large European study
5. Phenotype difference between ALS patients with expanded repeats inC9ORF72and patients with mutations in other ALS-related genes
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