4 results for author:"Reynolds T.R." in Literature citations
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| Structure of the human biotinidase gene. Knight H.C., Reynolds T.R., Meyers G.A., Pomponio R.J., Buck G.A., Wolf B. Mamm. Genome 9:327-330(1998) · UniProtKB (1) |
| Arg538 to Cys mutation in a CpG dinucleotide of the human biotinidase gene is the second most common cause of profound biotinidase deficiency in symptomatic children. Pomponio R.J., Norrgard K.J., Hymes J., Reynolds T.R., Buck G.A., Baumgartner R., Suormala T., Wolf B. Hum. Genet. 99:506-512(1997) · UniProtKB (1) |
| Mutational hotspot in the human biotinidase gene causes profound biotinidase deficiency. Pomponio R.J., Reynolds T.R., Cole H., Buck G.A., Wolf B. Nat. Genet. 11:96-98(1995) |
| Human serum biotinidase. cDNA cloning, sequence, and characterization. Cole H., Reynolds T.R., Lockyer J.M., Buck G.A., Denson T., Spence J.E., Hymes J., Wolf B. J. Biol. Chem. 269:6566-6570(1994) · UniProtKB (1) |