YUHSpace: Browsing DSpace

All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

가 나 다 라 마 바 사 아 자 차 카 타 파 하

Showing results 1 to 9 of 9

This table browses all dspace content
Issue Date	Title	Journal Title
2010	Association between survivor motor neuron 2 (SMN2) gene homozygous deletion and sporadic lower motor neuron disease in a Korean population.	ANNALS OF CLINICAL AND LABORATORY SCIENCE
2008	Becker muscular dystrophy with r(X) carrying an out-of-frame DMD deletion	PEDIATRIC NEUROLOGY
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
2012	Homozygous SMN2 deletion is a major risk factor among twenty-five Korean sporadic amyotrophic lateral sclerosis patients	YONSEI MEDICAL JOURNAL
2010	Multiplex Ligation-dependent Probe Amplification (MLPA) 방법에 의한 디스트로핀 유전자 돌연변이 분자학적 진단의 유용성	Journal of the Korean Neurological Association
2012	Population-specific spectrum of the F11 mutations in Koreans: evidence for a founder effect.	CLINICAL GENETICS
2005	Serotonin transporter gene polymorphism and migraine in the Korean population	HEADACHE
2010	Serum neuron-specific enolase level as a biomarker in differential diagnosis of seizure and syncope	JOURNAL OF NEUROLOGY
2011	Three cases of manifesting female carriers in patients with Duchenne muscular dystrophy.	YONSEI MEDICAL JOURNAL