Hamid Azzedine

1. Phenotypical Features of a Moroccan Family With Autosomal Recessive Charcot-Marie-Tooth Disease Associated With the S194X Mutation in the GDAP1 Gene
   2003/04/01 by Nazha Birouk, Hamid Azzedine, O. Dubourg +9 · 77 citations
   Neuroscience · Medicine · Biochemistry, Genetics and Molecular Biology · #Hereditary Neurological Disorders #Peripheral Neuropathies and Disorders #Nuclear Structure and Function #Pathological #Nerve biopsy #Pathology #Hereditary motor and sensory neuropathy #Mutation #Disease #Consanguinity #Phenotype #Medicine #Genetic heterogeneity #Biology #Degenerative disease #Genetics #Gene #Peripheral neuropathy #Endocrinology #Diabetes mellitus
2. Variability of disease progression in a family with autosomal recessive CMT associated with a S194X and new R310Q mutation in the GDAP1 gene
   2003/05/01 by H Azzedine, Hamid Azzedine, Merle Ruberg +15 · 44 citations
   Biochemistry, Genetics and Molecular Biology · Medicine · Neuroscience · #Allele #Biology #Cellular transport and secretion #Compound heterozygosity #Disease #Gene #Genetic Neurodegenerative Diseases #Genetics #Hereditary Neurological Disorders #Heterozygote advantage #Medicine #Mutation #Pathology #Phenotype