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Publications by Tarik Hamadouche
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
Related publications
A Severe Recessive and a Mild Dominant Form of Charcot-Marie-Tooth Disease Associated With a Newly Identified Glu222Lys GDAP1 Gene Mutation.
Acta Biochimica Polonica
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Molecular Biology
A Novel GJB1 Mutation Associated With X‐linked Charcot–Marie–Tooth Disease in a Large Chinese Family Pedigree
Molecular genetics & genomic medicine
Genetics
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The First De Novo Mutation of the Connexin 32 Gene Associated With X Linked Charcot-Marie-Tooth Disease.
Journal of Medical Genetics
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Autosomal Dominant Charcot-Marie-Tooth Disease Type 2A1
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2U
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2M
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2O
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2B
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2Q
