3 results for author:"Biery B.J." in Literature citations
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| Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia. Sacksteder K.A., Biery B.J., Morrell J.C., Goodman B.K., Geisbrecht B.V., Cox R.P., Gould S.J., Geraghty M.T. Am. J. Hum. Genet. 66:1736-1743(2000) · UniProtKB (1) |
| Gene structure and mutations of glutaryl-coenzyme A dehydrogenase: impaired association of enzyme subunits that is due to an A421V substitution causes glutaric acidemia type I in the Amish. Biery B.J., Stein D.E., Morton D.H., Goodman S.I. Am. J. Hum. Genet. 59:1006-1011(1996) · UniProtKB (1) |
| Cloning of glutaryl-CoA dehydrogenase cDNA, and expression of wild type and mutant enzymes in Escherichia coli. Goodman S.I., Kratz L.E., Digiulio K.A., Biery B.J., Goodman K.E., Isaya G., Frerman F.E. Hum. Mol. Genet. 4:1493-1498(1995) · UniProtKB (1) |