Niemann-Pick C1 disease: the I1061T substitution is a frequent mutant allele in patients of Western European descent and correlates with a classic juvenile phenotype.

MLA

Millat, G., et al. “Niemann-Pick C1 Disease: The I1061T Substitution Is a Frequent Mutant Allele in Patients of Western European Descent and Correlates with a Classic Juvenile Phenotype.” American Journal of Human Genetics, vol. 65, no. 5, Nov. 1999, pp. 1321–29. EBSCOhost, https://doi.org/10.1086/302626.

APA

Millat, G., Marçais, C., Rafi, M. A., Yamamoto, T., Morris, J. A., Pentchev, P. G., Ohno, K., Wenger, D. A., & Vanier, M. T. (1999). Niemann-Pick C1 disease: the I1061T substitution is a frequent mutant allele in patients of Western European descent and correlates with a classic juvenile phenotype. American Journal of Human Genetics, 65(5), 1321–1329. https://doi.org/10.1086/302626

Chicago

Millat, G, C Marçais, M A Rafi, T Yamamoto, J A Morris, P G Pentchev, K Ohno, D A Wenger, and M T Vanier. 1999. “Niemann-Pick C1 Disease: The I1061T Substitution Is a Frequent Mutant Allele in Patients of Western European Descent and Correlates with a Classic Juvenile Phenotype.” American Journal of Human Genetics 65 (5): 1321–29. doi:10.1086/302626.