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Charcot-marie-tooth disease: seventeen causative genes.
Lee JH, Choi BO. Lee JH, et al. Among authors: choi bo. J Clin Neurol. 2006 Jun;2(2):92-106. doi: 10.3988/jcn.2006.2.2.92. Epub 2006 Jun 20. J Clin Neurol. 2006. PMID: 20396492 Free PMC article.
Comparison between clinical disabilities and electrophysiological values in Charcot-Marie-Tooth 1A patients with PMP22 duplication.
Kim YH, Chung HK, Park KD, Choi KG, Kim SM, Sunwoo IN, Choi YC, Lim JG, Lee KW, Kim KK, Lee DK, Joo IS, Kwon KH, Gwon SB, Park JH, Kim DS, Kim SH, Kim WK, Suh BC, Kim SB, Kim NH, Sohn EH, Kim OJ, Kim HS, Cho JH, Kang SY, Park CI, Oh J, Shin JH, Chung KW, Choi BO. Kim YH, et al. Among authors: choi kg, choi bo, choi yc. J Clin Neurol. 2012 Jun;8(2):139-45. doi: 10.3988/jcn.2012.8.2.139. Epub 2012 Jun 29. J Clin Neurol. 2012. PMID: 22787498 Free PMC article.
SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3.
Nakhro K, Park JM, Hong YB, Park JH, Nam SH, Yoon BR, Yoo JH, Koo H, Jung SC, Kim HL, Kim JY, Choi KG, Choi BO, Chung KW. Nakhro K, et al. Among authors: choi kg, choi bo. Neurology. 2013 Jul 9;81(2):165-73. doi: 10.1212/WNL.0b013e31829a3421. Epub 2013 Jun 7. Neurology. 2013. PMID: 23749797
A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy.
Hong YB, Joo J, Hyun YS, Kwak G, Choi YR, Yeo HK, Jwa DH, Kim EJ, Mo WM, Nam SH, Kim SM, Yoo JH, Koo H, Park HT, Chung KW, Choi BO. Hong YB, et al. Among authors: choi bo, choi yr. PLoS Genet. 2016 Feb 1;12(2):e1005829. doi: 10.1371/journal.pgen.1005829. eCollection 2016 Feb. PLoS Genet. 2016. PMID: 26828946 Free PMC article.
754 results