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Genomics, v.89 no.4, 2007년, pp.512 - 520
Nag, Nabanita (Section on Molecular Structure and Functional Genomics, National Eye Institute, National Institutes of Health, Building 7, Room 201 Bethesda, MD 20892, USA) , Peterson, Katherine (Section on Molecular Structure and Functional Genomics, National Eye Institute, National Institutes of Health, Building 7, Room 201 Bethesda, MD 20892, USA) , Wyatt, Keith (Section on Molecular Structure and Functional Genomics, National Eye Institute, National Institutes of Health, Building 7, Room 201 Bethesda, MD 20892, USA) , Hess, Sonja (Proteomics and Mass Spectrometry Facility, NIDDK, National Institutes of Health, Bethesda, MD 20892, USA) , Ray, Sugata (Section on Molecular Structure and Functional Genomics, National Eye Institute, National Institutes of Health, Building 7, Room 201 Bethesda, MD 20892, USA) , Favor, Jack (Institute of Human Genetics, GSF-National Research Center for Environment and Health, Ingolstaedter Landstr. 1, D-85764 Neuherberg, Germany) , Bogani, Debora (Medical Research Council, Harwell, Didcot, OX11 0RD, UK) , Lyon, Mary (Medical Research Council, Harwell, Didcot, OX11 0RD, UK) , Wistow, Graeme (Sec)
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AbstractNo3 (nuclear opacity 3) is a novel congenital nuclear cataract in mice. Microsatellite mapping placed the No3 locus on chromosome 1 between D1Mit480 (32cM) and D1Mit7 (41cM), a region containing seven crystallin genes; Cryba2 and the Cryga-Crygf cluster. Although polymorphic variants were ob...
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