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NR2F1 mutations cause optic atrophy with intellectual disability.
Bosch DG, Boonstra FN, Gonzaga-Jauregui C, Xu M, de Ligt J, Jhangiani S, Wiszniewski W, Muzny DM, Yntema HG, Pfundt R, Vissers LE, Spruijt L, Blokland EA, Chen CA; Baylor-Hopkins Center for Mendelian Genomics; Lewis RA, Tsai SY, Gibbs RA, Tsai MJ, Lupski JR, Zoghbi HY, Cremers FP, de Vries BB, Schaaf CP. Bosch DG, et al. Among authors: tsai mj, tsai sy. Am J Hum Genet. 2014 Feb 6;94(2):303-9. doi: 10.1016/j.ajhg.2014.01.002. Epub 2014 Jan 23. Am J Hum Genet. 2014. PMID: 24462372 Free PMC article.
Coup d'Etat: an orphan takes control.
Lin FJ, Qin J, Tang K, Tsai SY, Tsai MJ. Lin FJ, et al. Among authors: tsai mj, tsai sy. Endocr Rev. 2011 Jun;32(3):404-21. doi: 10.1210/er.2010-0021. Epub 2011 Jan 21. Endocr Rev. 2011. PMID: 21257780 Free PMC article. Review.
840 results