Utility of whole exome sequencing for the early diagnosis of pediatric-onset cerebellar atrophy associated with developmental delay in an inbred population.

MLA

Megahed, Hisham, et al. “Utility of Whole Exome Sequencing for the Early Diagnosis of Pediatric-Onset Cerebellar Atrophy Associated with Developmental Delay in an Inbred Population.” Orphanet Journal of Rare Diseases, vol. 11, no. 1, May 2016, p. 57. EBSCOhost, https://doi.org/10.1186/s13023-016-0436-9.

APA

Megahed, H., Nicouleau, M., Barcia, G., Medina-Cano, D., Siquier-Pernet, K., Bole-Feysot, C., Parisot, M., Masson, C., Nitschké, P., Rio, M., Bahi-Buisson, N., Desguerre, I., Munnich, A., Boddaert, N., Colleaux, L., & Cantagrel, V. (2016). Utility of whole exome sequencing for the early diagnosis of pediatric-onset cerebellar atrophy associated with developmental delay in an inbred population. Orphanet Journal of Rare Diseases, 11(1), 57. https://doi.org/10.1186/s13023-016-0436-9

Chicago

Megahed, Hisham, Michaël Nicouleau, Giulia Barcia, Daniel Medina-Cano, Karine Siquier-Pernet, Christine Bole-Feysot, Mélanie Parisot, et al. 2016. “Utility of Whole Exome Sequencing for the Early Diagnosis of Pediatric-Onset Cerebellar Atrophy Associated with Developmental Delay in an Inbred Population.” Orphanet Journal of Rare Diseases 11 (1): 57. doi:10.1186/s13023-016-0436-9.