Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome.

MLA

Ghosh, Shereen G., et al. “Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome.” American Journal of Human Genetics, vol. 108, no. 12, Dec. 2021, p. 2385. EBSCOhost, https://doi.org/10.1016/j.ajhg.2021.11.013.

APA

Ghosh, S. G., Becker, K., Huang, H., Salazar, T. D., Chai, G., Salpietro, V., Al-Gazali, L., Waisfisz, Q., Wang, H., Vaux, K. K., Stanley, V., Manole, A., Akpulat, U., Weiss, M. M., Efthymiou, S., Hanna, M. G., Minetti, C., Striano, P., Pisciotta, L., … Gleeson, J. G. (2021). Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome. American Journal of Human Genetics, 108(12), 2385. https://doi.org/10.1016/j.ajhg.2021.11.013

Chicago

Ghosh, Shereen G, Kerstin Becker, He Huang, Tracy D Salazar, Guoliang Chai, Vincenzo Salpietro, Lihadh Al-Gazali, et al. 2021. “Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome.” American Journal of Human Genetics 108 (12): 2385. doi:10.1016/j.ajhg.2021.11.013.