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APA Citation
Guldberg, P., Levy, H. L., Henriksen, K. F., & Guttler, F. (1996). three prevalent mutations in a patient with phenylalanine hydroxylase deficiency: implications for diagnosis and genetic counselling.. Journal of medical genetics, 33(2), 161–164. http://access.bl.uk/ark:/81055/vdc_100135126497.0x000031