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Screening for MAPT and PGRN mutations in Korean patients with PSP/CBS/FTD.
Kim HJ, Jeon BS, Yun JY, Seong MW, Park SS, Lee JY. Kim HJ, et al. Among authors: seong mw. Parkinsonism Relat Disord. 2010 May;16(4):305-6. doi: 10.1016/j.parkreldis.2010.01.004. Epub 2010 Feb 19. Parkinsonism Relat Disord. 2010. PMID: 20171924 No abstract available.
Ophthalmoplegia diagnosis.
Hwang JM, Choung HK, Ko HS, Seong MW, Kim JY, Park SS. Hwang JM, et al. Among authors: seong mw. Ophthalmology. 2009 Apr;116(4):813-4, 814.e1-2. doi: 10.1016/j.ophtha.2008.12.006. Ophthalmology. 2009. PMID: 19344829 No abstract available.
Revisit of multiple epiphyseal dysplasia: ethnic difference in genotypes and comparison of radiographic features linked to the COMP and MATN3 genes.
Kim OH, Park H, Seong MW, Cho TJ, Nishimura G, Superti-Furga A, Unger S, Ikegawa S, Choi IH, Song HR, Kim HW, Yoo WJ, Shim JS, Chung CY, Oh CW, Jeong C, Song KS, Seo SG, Cho SI, Yeo IK, Kim SY, Park S, Park SS. Kim OH, et al. Among authors: seong mw. Am J Med Genet A. 2011 Nov;155A(11):2669-80. doi: 10.1002/ajmg.a.34246. Epub 2011 Sep 30. Am J Med Genet A. 2011. PMID: 21965141
239 results