Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia.

MLA

Husain, Ralf A., et al. “Bi-Allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia.” American Journal of Human Genetics, vol. 107, no. 2, Aug. 2020, pp. 364–73. EBSCOhost, https://doi.org/10.1016/j.ajhg.2020.06.015.

APA

Husain, R. A., Grimmel, M., Wagner, M., Hennings, J. C., Marx, C., Feichtinger, R. G., Saadi, A., Rostásy, K., Radelfahr, F., Bevot, A., Döbler-Neumann, M., Hartmann, H., Colleaux, L., Cordts, I., Kobeleva, X., Darvish, H., Bakhtiari, S., Kruer, M. C., Besse, A., & Ng, A. C.-H. (2020). Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia. American Journal of Human Genetics, 107(2), 364–373. https://doi.org/10.1016/j.ajhg.2020.06.015

Chicago

Husain, Ralf A., Mona Grimmel, Matias Wagner, J. Christopher Hennings, Christian Marx, René G. Feichtinger, Abdelkrim Saadi, et al. 2020. “Bi-Allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia.” American Journal of Human Genetics 107 (2): 364–73. doi:10.1016/j.ajhg.2020.06.015.