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Showing results 1 to 6 of 6

Issue Date	Title	Author(s)	Type
2006	A complex peripheral neuropathy family harboring CMT1A duplication and HNPP deletion	최병옥	Meeting Abstract
2007	A family harboring CMT1A duplication and HNPP deletion	최병옥	Article
2016	ADSSL1 mutation relevant to autosomal recessive adolescent onset distal myopathy	유정현; 정성철; 박형준	Article
2012	Comparison between Clinical Disabilities and Electrophysiological Values in Charcot-Marie-Tooth 1A Patients with PMP22 Duplication (vol 8, pg 139, 2012)	최경규; 박기덕; 최병옥; 김영화	Correction
2006	Early onset severe and late onset mild Charcot-Marie-Tooth disease with mitofusin 2 (MFN2) mutations	최경규; 박기덕; 최병옥	Meeting Abstract
2016	Recessive optic atrophy, sensorimotor neuropathy and cataract associated with novel compound heterozygous mutations in OPA1	구혜수; 유정현; 정성철	Article

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