Okamoto, N., Naruto, T., Kohmoto, T., Komori, T., & Imoto, I. (2014). A novel PTCH1 mutation in a patient with Gorlin syndrome. Human genome variation, 1(1), 14022. https://doi.org/10.1038/hgv.2014.22
Chicago Style (17th ed.) CitationOkamoto, Nana, Takuya Naruto, Tomohiro Kohmoto, Takahide Komori, and Issei Imoto. "A Novel PTCH1 Mutation in a Patient with Gorlin Syndrome." Human Genome Variation 1, no. 1 (2014): 14022. https://doi.org/10.1038/hgv.2014.22.
MLA (9th ed.) CitationOkamoto, Nana, et al. "A Novel PTCH1 Mutation in a Patient with Gorlin Syndrome." Human Genome Variation, vol. 1, no. 1, 2014, p. 14022, https://doi.org/10.1038/hgv.2014.22.
Warning: These citations may not always be 100% accurate.