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Showing results 1 to 5 of 5

Issue Date	Title / Author(s) / Citation	File	Altmetrics
2009-01	Molecular and clinical characteristics of myotonic dystrophy type 1 in koreans Kim, So Yeon; Kim, Ji Yeon; Kim, Gyoung Pyoung; Sung, Jung-Jun; Lim, Kyu Sang; Lee, Kwang-Woo; Chae, Jong Hee; Hong, Yoon-Ho; Seong, Moon-Woo; Park, Sung Sup Korean J Lab Med. 2008;28(6):483-492	view file link
2009-03	The G2019S LRRK2 Mutation is Rare in Korean Patients with Parkinson`s Disease and Multiple System Atrophy Cho, Jin-Whan; Kim, Sung-Yeon; Park, Sung-Sup; Jeon, Beom S. JOURNAL OF CLINICAL NEUROLOGY; Vol.5 1; 29-32	view file DOI
2010-05	Screening for MAPT and PGRN mutations in Korean patients with PSP/CBS/FTD Kim, Han-Joon; Jeon, Beom S.; Yun, Ji Young; Seong, Moon-Woo; Lee, Jee-Young; Park, Sung Sup PARKINSONISM & RELATED DISORDERS; Vol.16(4); 305-306	DOI
2012-08	A novel double mutation in cis in MFN2 causes Charcot-Marie-Tooth neuropathy type 2A Park, Su-Yeon; Kim, So Yeon; Hong, Yoon-Ho; Cho, Sung Im; Seong, Moon-Woo; Park, Sung Sup NEUROGENETICS Vol.13 No.3, pp. 275-280	DOI
2019-03	The Korean undiagnosed diseases program: lessons from a one-year pilot project Kim, Soo Yeon; Lim, Byung Chan; Lee, Jin Sook; Kim, Woo Joong; Kim, Hyuna; Ko, Jung Min; Kim, Ki Joong; Choi, Sun Ah; Kim, Hunmin; Hwang, Hee; Choi, Ji Eun; Cho, Anna; Moon, Jangsup; Seong, Moon Woo; Park, Sung Sup; Lee, Yun Jeong; Kim, Young Ok; Kim, Jon Soo; Kim, Won Seop; Kwon, Young Se; Park, June Dong; Ahn, Younjhin; Hwang, Joo-Yeon; Park, Hyun-Young; Lee, Youngha; Choi, Murim; Chae, Jong-Hee Orphanet Journal of Rare Diseases. 2019 Mar 20;14(1):68	view file DOI

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