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Charcot-Marie-Tooth Disease Type 1A — Gene Therapy & Clinical Trials | FollowGene
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Charcot-Marie-Tooth Disease Type 1A
Charcot-Marie-Tooth Disease Type 1A
Prevalence:
1/5000
neurological
Official
·
OMIM:118220
Official
·
ORPHA101081
Peripheral neuropathy caused by PMP22 gene duplication.
Associated Genes
PMP22
Peripheral Myelin Protein 22
Chromosome 17
Autosomal Dominant