5 results on '"Humbertclaude, Véronique"'
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2. Severe phenotypic spectrum of biallelic mutations in PRRT2 gene
3. Genotype-Phenotype Analysis in 2,405 Patients with a Dystrophinopathy Using the UMD-DMD Database: A Model of Nationwide Knowledgebase
4. Multiexon Skipping Leading to an Artificial DMD Protein Lacking Amino Acids from Exons 45 Through 55 Could Rescue Up to 63% of Patients With Duchenne Muscular Dystrophy
5. Interictal Paroxysmal Epileptic Discharges during Sleep in Childhood: Phenotypic Variability in a Family
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