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Publications by H Rouger
The First De Novo Mutation of the Connexin 32 Gene Associated With X Linked Charcot-Marie-Tooth Disease.
Journal of Medical Genetics
Genetics
Related publications
Transient, Recurrent, White Matter Lesions in X-Linked Charcot-Marie-Tooth Disease With Novel Connexin 32 Mutation
Archives of Neurology
X-Linked Charcot-Marie-Tooth Disease Type 3
A Novel GJB1 Mutation Associated With X‐linked Charcot–Marie–Tooth Disease in a Large Chinese Family Pedigree
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Charcot–Marie–Tooth Disease
Phenotypical Features of a Moroccan Family With Autosomal Recessive Charcot-Marie-Tooth Disease Associated With the S194X Mutation in the GDAP1 Gene
Archives of Neurology
Charcot-Marie-Tooth Disease Type 2R
Update on Charcot-Marie-Tooth Disease
Current Neurology and Neuroscience Reports
Neuroscience
Neurology
Charcot-Marie-Tooth Disease Type 2B5
Charcot-Marie-Tooth Disease Type 4G
