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Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy.
Minassian BA, Lee JR, Herbrick JA, Huizenga J, Soder S, Mungall AJ, Dunham I, Gardner R, Fong CY, Carpenter S, Jardim L, Satishchandra P, Andermann E, Snead OC 3rd, Lopes-Cendes I, Tsui LC, Delgado-Escueta AV, Rouleau GA, Scherer SW. Minassian BA, et al. Among authors: lee jr. Nat Genet. 1998 Oct;20(2):171-4. doi: 10.1038/2470. Nat Genet. 1998. PMID: 9771710
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Osborne LR, Lee JR, Scherer SW. Osborne LR, et al. Among authors: lee jr. Mol Med Today. 1997 Sep;3(9):370-3. doi: 10.1016/S1357-4310(97)82918-8. Mol Med Today. 1997. PMID: 9302686
Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site.
Mishmar D, Rahat A, Scherer SW, Nyakatura G, Hinzmann B, Kohwi Y, Mandel-Gutfroind Y, Lee JR, Drescher B, Sas DE, Margalit H, Platzer M, Weiss A, Tsui LC, Rosenthal A, Kerem B. Mishmar D, et al. Among authors: lee jr. Proc Natl Acad Sci U S A. 1998 Jul 7;95(14):8141-6. doi: 10.1073/pnas.95.14.8141. Proc Natl Acad Sci U S A. 1998. PMID: 9653154 Free PMC article.
Molecular analysis of the PDS gene in Pendred syndrome.
Coyle B, Reardon W, Herbrick JA, Tsui LC, Gausden E, Lee J, Coffey R, Grueters A, Grossman4 A, Phelps PD, Luxon L, Kendall-Taylor P, Scherer SW, Trembath RC. Coyle B, et al. Hum Mol Genet. 1998 Jul;7(7):1105-12. doi: 10.1093/hmg/7.7.1105. Hum Mol Genet. 1998. PMID: 9618167
1,963 results