A gel electrophoretic assay for detecting the insertion defect in Ashkenazi Jewish carriers of Tay-Sachs disease.
暂无分享,去创建一个
[1] R. Myerowitz,et al. The major defect in Ashkenazi Jews with Tay-Sachs disease is an insertion in the gene for the alpha-chain of beta-hexosaminidase. , 1988, The Journal of biological chemistry.
[2] S. Schuster,et al. Identification of an altered splice site in Ashkenazi Tay-Sachs disease , 1988, Nature.
[3] R. Terlevich,et al. A supernova in the nucleus of NGC5548? , 1988, Nature.
[4] R. Proia,et al. Organization of the gene encoding the human beta-hexosaminidase alpha-chain. , 1987, The Journal of biological chemistry.
[5] S. Garger,et al. Rapid purification of plasmid DNA by a single centrifugation in a two-step cesium chloride-ethidium bromide gradient. , 1983, Biochemical and biophysical research communications.
[6] Charles R.scriver. The Metabolic basis of inherited disease , 1989 .
[7] S. Colowick,et al. Methods in Enzymology , Vol , 1966 .