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Biochemical and molecular characterisation of neurological Wilson disease.
Seo GH, Kim YM, Oh SH, Chung SJ, Choi IH, Kim GH, Yum MS, Choi JH, Kim KM, Ko TS, Lee BH, Yoo HW. Seo GH, et al. Among authors: kim gh, kim km, kim ym. J Med Genet. 2018 Sep;55(9):587-593. doi: 10.1136/jmedgenet-2017-105214. Epub 2018 Apr 4. J Med Genet. 2018. PMID: 29618506
Focal hand dystonia in a patient with PANK2 mutation.
Chung SJ, Lee JH, Lee MC, Yoo HW, Kim GH. Chung SJ, et al. Among authors: kim gh. Mov Disord. 2008 Feb 15;23(3):466-8. doi: 10.1002/mds.21880. Mov Disord. 2008. PMID: 18074375 No abstract available.
Clinical characteristics and mutation spectrum of GLA in Korean patients with Fabry disease by a nationwide survey: Underdiagnosis of late-onset phenotype.
Choi JH, Lee BH, Heo SH, Kim GH, Kim YM, Kim DS, Ko JM, Sohn YB, Hong YH, Lee DH, Kook H, Lim HH, Kim KH, Kim WS, Hong GR, Kim SH, Park SH, Kim CD, Kim SM, Seo JS, Yoo HW. Choi JH, et al. Among authors: kim ds, kim gh, kim cd, kim ym, kim sh, kim sm, kim ws, kim kh. Medicine (Baltimore). 2017 Jul;96(29):e7387. doi: 10.1097/MD.0000000000007387. Medicine (Baltimore). 2017. PMID: 28723748 Free PMC article.
2,253 results