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Systematic analysis of inheritance pattern determination in genes that cause rare neurodevelopmental diseases.
Park S, Jang SS, Lee S, Kim M, Sim H, Jeon H, Hong SE, Lee J, Lee J, Jeon EY, Lee J, Lee CR, Kim SY, Kim MJ, Yoon JG, Lim BC, Kim WJ, Kim KJ, Ko JM, Cho A, Lee JS, Choi M, Chae JH. Park S, et al. Among authors: kim kj, kim wj, kim sy, kim m, kim mj. Front Genet. 2022 Sep 12;13:990015. doi: 10.3389/fgene.2022.990015. eCollection 2022. Front Genet. 2022. PMID: 36212160 Free PMC article.
Childhood ocular myasthenia gravis.
Kim JH, Hwang JM, Hwang YS, Kim KJ, Chae J. Kim JH, et al. Among authors: kim kj. Ophthalmology. 2003 Jul;110(7):1458-62. doi: 10.1016/S0161-6420(03)00460-3. Ophthalmology. 2003. PMID: 12867410
Clinical features of A3243G mitochondrial tRNA mutation.
Chae JH, Hwang H, Lim BC, Cheong HI, Hwang YS, Kim KJ. Chae JH, et al. Among authors: kim kj. Brain Dev. 2004 Oct;26(7):459-62. doi: 10.1016/j.braindev.2004.01.002. Brain Dev. 2004. PMID: 15351082
Merosin-deficient congenital muscular dystrophy in Korea.
Chae JH, Lee JS, Hwang H, Kim KJ, Hwang YS, Park JD, Cheon JE, Kim IO, Choe GY, Park SH. Chae JH, et al. Among authors: kim kj, kim io. Brain Dev. 2009 May;31(5):341-6. doi: 10.1016/j.braindev.2008.06.009. Epub 2008 Aug 23. Brain Dev. 2009. PMID: 18723302
Cerebellum can be a possible generator of progressive myoclonus.
Koh KN, Lim BC, Hwang H, Park JD, Chae JH, Kim KJ, Hwang YS, Kim SK, Wang KC, Moon HK. Koh KN, et al. Among authors: kim kj, kim sk. J Child Neurol. 2010 Jun;25(6):728-31. doi: 10.1177/0883073809342273. Epub 2009 Sep 22. J Child Neurol. 2010. PMID: 19773463
3,114 results