Wiman, Å., Floderus, Y., & Harper, P. (2002). Two novel mutations and coexistence of the 991C.T and the 1339C.T mutation on a single allele in the coproporphyrinogen oxidase gene in Swedish patients with hereditary coproporphyria. Journal of Human Genetics, 47(8), 407.
Chicago Style (17th ed.) CitationWiman, Å, Y. Floderus, and P. Harper. "Two Novel Mutations and Coexistence of the 991C.T and the 1339C.T Mutation on a Single Allele in the Coproporphyrinogen Oxidase Gene in Swedish Patients with Hereditary Coproporphyria." Journal of Human Genetics 47, no. 8 (2002): 407.
MLA (9th ed.) CitationWiman, Å, et al. "Two Novel Mutations and Coexistence of the 991C.T and the 1339C.T Mutation on a Single Allele in the Coproporphyrinogen Oxidase Gene in Swedish Patients with Hereditary Coproporphyria." Journal of Human Genetics, vol. 47, no. 8, 2002, p. 407.