De novo SHANK3 mutation causes Rett syndrome-like phenotype in a female patient.

MLA

Hara, Munetsugu, et al. “De Novo SHANK3 Mutation Causes Rett Syndrome-like Phenotype in a Female Patient.” American Journal of Medical Genetics. Part A, vol. 167, no. 7, July 2015, pp. 1593–96. EBSCOhost, https://doi.org/10.1002/ajmg.a.36775.

APA

Hara, M., Ohba, C., Yamashita, Y., Saitsu, H., Matsumoto, N., & Matsuishi, T. (2015). De novo SHANK3 mutation causes Rett syndrome-like phenotype in a female patient. American Journal of Medical Genetics. Part A, 167(7), 1593–1596. https://doi.org/10.1002/ajmg.a.36775

Chicago

Hara, Munetsugu, Chihiro Ohba, Yushiro Yamashita, Hirotomo Saitsu, Naomichi Matsumoto, and Toyojiro Matsuishi. 2015. “De Novo SHANK3 Mutation Causes Rett Syndrome-like Phenotype in a Female Patient.” American Journal of Medical Genetics. Part A 167 (7): 1593–96. doi:10.1002/ajmg.a.36775.