Showing results 1 to 5 of 5
Issue Date | Title | Author(s) | Type |
---|---|---|---|
2014 | A cohort study of MFN2 mutations and phenotypic spectrums in Charcot-Marie-Tooth disease 2A patients | 정성철 | Article in Press |
2011 | A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14 | 최경규; 구혜수; 박기덕; 유정현; 최병옥 | Article |
2018 | Association of miR-149 polymorphism with onset age and severity in Charcot–Marie–Tooth disease type 1A | 정성철 | Article |
2011 | MPZ mutation in an early-onset Charcot-Marie-Tooth disease type 1B family by genome-wide linkage analysis | 최경규; 구혜수; 박기덕; 유정현; 최병옥 | Article |
2011 | Wide phenotypic variations in Charcot-Marie-Tooth 1A neuropathy with rare copy number variations on 17p12 | 구혜수; 최병옥 | Article |