Increased plasma pyridoxal-5′-phosphate levels before and after pyridoxine loading in carriers of perinatal/infantile hypophosphatasia

Author:

Chodirker B. N.,Coburn S. P.,Seargeant L. E.,Whyte M. P.,Greenberg C. R.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference13 articles.

1. Chodirker, B. N., Evans, J. A., Seargeant, L. E., Cheang, M. S. and Greenberg, C. R. Hypophosphatemia in infantile hypophosphatasia: Implications for carrier diagnosis and screening.Am. J. Hum. Genet. 46 (1990) 280–285

2. Coburn, S. P. and Mahuren, J. D. A versatile cation-exchange procedure for measuring the seven major forms of vitamin B6 in biological samples.Anal. Biochem. 129 (1983) 310–317

3. Coburn, S. P. and Whyte, M. P. Role of phosphatases in the regulation of vitamin B6 metabolism in hypophosphatasia and other disorders. In Leklem, J. E. and Reynolds, R. D. (eds.),Clinical and Physiological Applications of Vitamin B6, Liss, New York, 1988, pp. 65–93

4. Fedde, K. N., Lane, C. C. and Whyte, M. P. Alkaline phosphatase is an ectoenzyme which degrades natural substrates at micromolar concentration and physiologic pH in human osteosarcoma (SAOS-2) cells.Arch. Biochem. Biophys. 264 (1988) 400–409

5. Fraser, D. Hypophosphatasia.Am. J. Med. 22 (1957) 730–746

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