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A Unique Mutational Spectrum of MLC1 in Korean Patients With Megalencephalic Leukoencephalopathy With Subcortical Cysts: p.Ala275Asp Founder Mutation and Maternal Uniparental Disomy of Chromosome 22.
Choi SA, Kim SY, Yoon J, Choi J, Park SS, Seong MW, Kim H, Hwang H, Choi JE, Chae JH, Kim KJ, Kim S, Lee YJ, Nam SO, Lim BC. Choi SA, et al. Among authors: kim kj, kim h, kim sy, kim s. Ann Lab Med. 2017 Nov;37(6):516-521. doi: 10.3343/alm.2017.37.6.516. Ann Lab Med. 2017. PMID: 28840990 Free PMC article.
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
New antiepileptic drugs in pediatric epilepsy.
Hwang H, Kim KJ. Hwang H, et al. Among authors: kim kj. Brain Dev. 2008 Oct;30(9):549-55. doi: 10.1016/j.braindev.2008.01.007. Epub 2008 Mar 6. Brain Dev. 2008. PMID: 18328657
Epilepsy surgery in children: outcomes and complications.
Kim SK, Wang KC, Hwang YS, Kim KJ, Chae JH, Kim IO, Cho BK. Kim SK, et al. Among authors: kim kj, kim io. J Neurosurg Pediatr. 2008 Apr;1(4):277-83. doi: 10.3171/PED/2008/1/4/277. J Neurosurg Pediatr. 2008. PMID: 18377302
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
3,119 results