Bayat, A., Christensen, M., Wibrand, F., Duno, M., & Lund, A. (2014). Mild Lesch–Nyhan Disease in a Boy with a Null Mutation in HPRT1: An Exception to the Known Genotype–Phenotype Correlation. JIMD Rep.
استشهاد بنمط شيكاغوBayat, Allan, Mette Christensen, Flemming Wibrand, Morten Duno, و Allan Lund. "Mild Lesch–Nyhan Disease in a Boy With a Null Mutation in HPRT1: An Exception to the Known Genotype–Phenotype Correlation." JIMD Rep 2014.
MLA استشهادBayat, Allan, et al. "Mild Lesch–Nyhan Disease in a Boy With a Null Mutation in HPRT1: An Exception to the Known Genotype–Phenotype Correlation." JIMD Rep 2014.
تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.