Showing results 9 to 13 of 13
Issue Date | Title | Author(s) | Type |
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2004 | Hereditary neuropathy with liability to pressure palsies (HNPP) patients of Korean ancestry with chromosome 17p11.2-p12 deletion | 박기덕; 최병옥 | Article |
2003 | Homozygous C677T mutation in the MTHFR gene as an independent risk factor for multiple small-artery occlusions | 최병옥 | Article |
2003 | Hyperhomocysteinemia as an independent risk factor for silent brain infarction | 최경규; 최병옥 | Article |
2004 | Mutational analysis of PMP22, MPZ, GJB1, EGR2 and NEFL in Korean Charcot-Marie-Tooth neuropathy patients. | 최경규; 최병옥 | Article |
2005 | Two missense mutations of EGR2 R359W and GJB1 V136A in a Charcot-Marie-Tooth disease family | 김원기; 구혜수; 박기덕; 최병옥 | Article |