Cite
Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: new mutations and the paradox between genotype and phenotype.
MLA
Keulemans, J. L., et al. “Human Alpha-N-Acetylgalactosaminidase (Alpha-NAGA) Deficiency: New Mutations and the Paradox between Genotype and Phenotype.” Journal of Medical Genetics, vol. 33, no. 6, June 1996, pp. 458–64. EBSCOhost, https://doi.org/10.1136/jmg.33.6.458.
APA
Keulemans, J. L., Reuser, A. J., Kroos, M. A., Willemsen, R., Hermans, M. M., van den Ouweland, A. M., de Jong, J. G., Wevers, R. A., Renier, W. O., Schindler, D., Coll, M. J., Chabas, A., Sakuraba, H., Suzuki, Y., & van Diggelen, O. P. (1996). Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: new mutations and the paradox between genotype and phenotype. Journal of Medical Genetics, 33(6), 458–464. https://doi.org/10.1136/jmg.33.6.458
Chicago
Keulemans, J L, A J Reuser, M A Kroos, R Willemsen, M M Hermans, A M van den Ouweland, J G de Jong, et al. 1996. “Human Alpha-N-Acetylgalactosaminidase (Alpha-NAGA) Deficiency: New Mutations and the Paradox between Genotype and Phenotype.” Journal of Medical Genetics 33 (6): 458–64. doi:10.1136/jmg.33.6.458.