Showing results 6 to 8 of 8
Issue Date | Title | Author(s) | Type |
---|---|---|---|
2013 | Rare variants in methionyl- and tyrosyl-tRNA synthetase genes in late-onset autosomal dominant Charcot-Marie-Tooth neuropathy | 최병옥 | Article in Press |
2014 | Recessive C10orf2 mutations in a family with infantile-onset spinocerebellar ataxia, sensorimotor polyneuropathy, and myopathy | 구혜수; 유정현 | Article |
2013 | SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3 | 김형래; 최경규; 구혜수; 유정현; 최병옥; 정성철 | Article |