APA (7th ed.) Citation

Canbek, S., & Şenol, M. G. (2024). Homozygous germline c.3380C>G missense mutation in PNPLA6 gene in a case of Gordon Holmes syndrome associated with hypogonadotropic hypogonadism, cerebellar ataxia, and juvenile type tremor. Journal of Neurosciences in Rural Practice, 15(4), 1. https://doi.org/10.25259/JNRP_24_2024

Chicago Style (17th ed.) Citation

Canbek, Sezin, and Mehmet Guney Şenol. "Homozygous Germline C.3380C>G Missense Mutation in PNPLA6 Gene in a Case of Gordon Holmes Syndrome Associated with Hypogonadotropic Hypogonadism, Cerebellar Ataxia, and Juvenile Type Tremor." Journal of Neurosciences in Rural Practice 15, no. 4 (2024): 1. https://doi.org/10.25259/JNRP_24_2024.

MLA (9th ed.) Citation

Canbek, Sezin, and Mehmet Guney Şenol. "Homozygous Germline C.3380C>G Missense Mutation in PNPLA6 Gene in a Case of Gordon Holmes Syndrome Associated with Hypogonadotropic Hypogonadism, Cerebellar Ataxia, and Juvenile Type Tremor." Journal of Neurosciences in Rural Practice, vol. 15, no. 4, 2024, p. 1, https://doi.org/10.25259/JNRP_24_2024.