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Results 1-9 of 9 (Search time: 0.0 seconds).
Item hits:
Issue Date
Title
Author(s)
Type
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
2010
Myofibrillar myopathy: A case report
구혜수; 박기덕
Article
2017
A longitudinal clinicopathological study of two unrelated patients with Charcot-Marie-Tooth disease type 1E
구혜수; 박기덕
Letter
2016
Genotype-phenotype correlation of Charcot-Marie-Tooth type 1E patients with PMP22 mutations
구혜수; 박기덕
Article
2013
Clinical and histopathological study of Charcot-Marie-Tooth neuropathy with a novel S90W mutation in BSCL2
최경규; 구혜수; 박기덕; 최병옥
Article
2017
Electron Microscopy Pathology of ADSSL1 Myopathy
구혜수; 박기덕; 유정현; 한수정
Letter
2016
Recurrent Episodes of Rhabdomyolysis after Seizures in a Patient with Glycogen Storage Disease Type V
구혜수; 박기덕; 이지은; 박형준
Letter
2013
Proximal dominant hereditary motor and sensory neuropathy with proximal dominance association with mutation in the TRK-fused gene
구혜수; 박기덕; 유정현; 최병옥; 정성철
Article
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