Heterozygous gain of function variants in a critical region of RNF13 cause congenital microcephaly, epileptic encephalopathy, blindness, and failure to thrive.

MLA

Taylor, Alan, et al. “Heterozygous Gain of Function Variants in a Critical Region of RNF13 Cause Congenital Microcephaly, Epileptic Encephalopathy, Blindness, and Failure to Thrive.” American Journal of Medical Genetics. Part A, vol. 191, no. 11, Nov. 2023, pp. 2723–27. EBSCOhost, https://doi.org/10.1002/ajmg.a.63390.

APA

Taylor, A., Kashyape, P. S., Jain, R., El Naofal, M., & Tayoun, A. A. (2023). Heterozygous gain of function variants in a critical region of RNF13 cause congenital microcephaly, epileptic encephalopathy, blindness, and failure to thrive. American Journal of Medical Genetics. Part A, 191(11), 2723–2727. https://doi.org/10.1002/ajmg.a.63390

Chicago

Taylor, Alan, Pawan S. Kashyape, Ruchi Jain, Maha El Naofal, and Ahmad Abou Tayoun. 2023. “Heterozygous Gain of Function Variants in a Critical Region of RNF13 Cause Congenital Microcephaly, Epileptic Encephalopathy, Blindness, and Failure to Thrive.” American Journal of Medical Genetics. Part A 191 (11): 2723–27. doi:10.1002/ajmg.a.63390.