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Issue Date | Title | Author(s) | Type |
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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 | 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 |
2013 | SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3 | 김형래; 최경규; 구혜수; 유정현; 최병옥; 정성철 | Article |