OA, B., HJ, C., A, C., JE, W., CR, S., & F, S. (2002). Variant Gaucher disease characterized by dysmorphic features, absence of cardiovascular involvement, laryngospasm, and compound heterozygosity for a novel mutation (D409H/C16S). American journal of medical genetics, 109(4), 328. https://doi.org/10.1002/ajmg.10385
Chicago Style (17th ed.) CitationOA, Bodamer, Church HJ, Cooper A, Wraith JE, Scott CR, and Scaglia F. "Variant Gaucher Disease Characterized by Dysmorphic Features, Absence of Cardiovascular Involvement, Laryngospasm, and Compound Heterozygosity for a Novel Mutation (D409H/C16S)." American Journal of Medical Genetics 109, no. 4 (2002): 328. https://doi.org/10.1002/ajmg.10385.
MLA (9th ed.) CitationOA, Bodamer, et al. "Variant Gaucher Disease Characterized by Dysmorphic Features, Absence of Cardiovascular Involvement, Laryngospasm, and Compound Heterozygosity for a Novel Mutation (D409H/C16S)." American Journal of Medical Genetics, vol. 109, no. 4, 2002, p. 328, https://doi.org/10.1002/ajmg.10385.