Results 1-6 of 6 (Search time: 0.0 seconds).
Issue Date | Title | Author(s) | Type |
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2016 | A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy | 구혜수; 유정현 | Article |
2016 | Genotype-phenotype correlation of Charcot-Marie-Tooth type 1E patients with PMP22 mutations | 구혜수; 박기덕 | Article |
2016 | Recurrent Episodes of Rhabdomyolysis after Seizures in a Patient with Glycogen Storage Disease Type V | 구혜수; 박기덕; 이지은; 박형준 | Letter |
2016 | A case of disseminated multidrug-resistant tuberculosis involving the brain | 구혜수; 최희정; 서의교 | Article |
2016 | Recessive optic atrophy, sensorimotor neuropathy and cataract associated with novel compound heterozygous mutations in OPA1 | 구혜수; 유정현; 정성철 | Article |
2016 | DGAT2 Mutation in a Family with Autosomal-Dominant Early-Onset Axonal Charcot-Marie-Tooth Disease | 구혜수; 정성철 | Article |