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Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
Kim HG, Kurth I, Lan F, Meliciani I, Wenzel W, Eom SH, Kang GB, Rosenberger G, Tekin M, Ozata M, Bick DP, Sherins RJ, Walker SL, Shi Y, Gusella JF, Layman LC. Kim HG, et al. Among authors: eom sh. Am J Hum Genet. 2008 Oct;83(4):511-9. doi: 10.1016/j.ajhg.2008.09.005. Epub 2008 Oct 2. Am J Hum Genet. 2008. PMID: 18834967 Free PMC article.
Structural studies on Helicobacter pyloriATP-dependent protease, FtsH.
Kim SH, Kang GB, Song HE, Park SJ, Bea MH, Eom SH. Kim SH, et al. Among authors: eom sh. J Synchrotron Radiat. 2008 May;15(Pt 3):208-10. doi: 10.1107/S090904950706846X. Epub 2008 Apr 18. J Synchrotron Radiat. 2008. PMID: 18421140 Free PMC article.
272 results