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Year Number of Results
2005 1
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2009 2
2011 1
2013 1
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2019 6
2021 5
2022 3
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2024 0

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Page 1
TNNT1 myopathy with novel compound heterozygous mutations.
Lee S, Eum J, Park S, Ki S, Hwang BJ, Kee Y, Chae JH. Lee S, et al. Among authors: kee y. Neuromuscul Disord. 2022 Feb;32(2):176-184. doi: 10.1016/j.nmd.2021.12.003. Epub 2021 Dec 16. Neuromuscul Disord. 2022. PMID: 35165004
Histopathological assessment of laterality defects in zebrafish development.
Chowdhury MAU, Raslan AA, Lee E, Eum J, Hwang BJ, Kwon SH, Kee Y. Chowdhury MAU, et al. Among authors: kee y. Anim Cells Syst (Seoul). 2021 May 26;25(3):136-145. doi: 10.1080/19768354.2021.1931443. eCollection 2021. Anim Cells Syst (Seoul). 2021. PMID: 34262656 Free PMC article.
The Korean undiagnosed diseases program phase I: expansion of the nationwide network and the development of long-term infrastructure.
Kim SY, Lee S, Woo H, Han J, Ko YJ, Shim Y, Park S, Jang SS, Lim BC, Ko JM, Kim KJ, Cho A, Kim H, Hwang H, Choi JE, Kim MJ, Moon J, Seong MW, Park SS, Choi SA, Lee JE, Kwon YS, Sohn YB, Kim JS, Kim WS, Lee YJ, Kwon S, Kim YO, Kook H, Cho YG, Cheon CK, Kang KS, Song MR, Kim YJ, Cha HJ, Choi HJ, Kee Y, Park SG, Baek ST, Choi M, Ryu DS, Chae JH. Kim SY, et al. Among authors: kee y. Orphanet J Rare Dis. 2022 Oct 8;17(1):372. doi: 10.1186/s13023-022-02520-5. Orphanet J Rare Dis. 2022. PMID: 36209187 Free PMC article.
25 results