Kelley-Seegmiller syndrome due to a unique variant of hypoxanthine-guanine phosphoribosyltransferase: reduced affinity for 5-phosphoribosyl-1-pyrophosphate manifested only at low, physiological substrate concentrations.

MLA

Zoref-Shani, E., et al. “Kelley-Seegmiller Syndrome Due to a Unique Variant of Hypoxanthine-Guanine Phosphoribosyltransferase: Reduced Affinity for 5-Phosphoribosyl-1-Pyrophosphate Manifested Only at Low, Physiological Substrate Concentrations.” Biochimica et Biophysica Acta, vol. 1500, no. 2, Feb. 2000, pp. 197–203. EBSCOhost, https://doi.org/10.1016/s0925-4439(99)00103-9.

APA

Zoref-Shani, E., Feinstein, S., Frishberg, Y., Bromberg, Y., & Sperling, O. (2000). Kelley-Seegmiller syndrome due to a unique variant of hypoxanthine-guanine phosphoribosyltransferase: reduced affinity for 5-phosphoribosyl-1-pyrophosphate manifested only at low, physiological substrate concentrations. Biochimica et Biophysica Acta, 1500(2), 197–203. https://doi.org/10.1016/s0925-4439(99)00103-9

Chicago

Zoref-Shani, E, S Feinstein, Y Frishberg, Y Bromberg, and O Sperling. 2000. “Kelley-Seegmiller Syndrome Due to a Unique Variant of Hypoxanthine-Guanine Phosphoribosyltransferase: Reduced Affinity for 5-Phosphoribosyl-1-Pyrophosphate Manifested Only at Low, Physiological Substrate Concentrations.” Biochimica et Biophysica Acta 1500 (2): 197–203. doi:10.1016/s0925-4439(99)00103-9.