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Issue Date	Title	Journal Title
2022	ATP1A2 유전자 변이를 보인 산발반신마비 편두통	Journal of the Korean Neurological Association(대한신경과학회지)
2024	Clinical Application of Optical Genome Mapping for Molecular Diagnosis of Facioscapulohumeral Muscular Dystrophy	ANNALS OF LABORATORY MEDICINE
2020	Hereditary Spastic Paraplegia with Axonal Sensorimotor Polyneuropathy in a Korean Family Caused by Pathogenic Variant of KIF5A (c.611G>A)	JOURNAL OF CLINICAL NEUROLOGY