Late-onset Charcot-Marie-Tooth type 2 disease with hearing impairment associated with a novel Pro105Thr mutation in theMPZ gene
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference12 articles.
1. Molecular genetics of autosomal-recessive axonal Charcot-Marie-Tooth neuropathies
2. The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot–Marie–Tooth phenotype
3. Charcot–Marie–Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene
4. A novel MPZ gene mutation in congenital neuropathy with hypomyelination
5. Charcot-Marie-Tooth families in Japan with MPZ Thr124Met mutation
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