Browsing byAuthorKanwal S.

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Showing results 1 to 5 of 5

Issue DateTitleAuthor(s)Type
2014A cohort study of MFN2 mutations and phenotypic spectrums in Charcot-Marie-Tooth disease 2A patients정성철Article in Press
2011A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14최경규; 구혜수; 박기덕; 유정현; 최병옥Article
2018Association of miR-149 polymorphism with onset age and severity in Charcot–Marie–Tooth disease type 1A정성철Article
2011MPZ mutation in an early-onset Charcot-Marie-Tooth disease type 1B family by genome-wide linkage analysis최경규; 구혜수; 박기덕; 유정현; 최병옥Article
2011Wide phenotypic variations in Charcot-Marie-Tooth 1A neuropathy with rare copy number variations on 17p12구혜수; 최병옥Article

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