APA (7th ed.) Citation

Elhennawy, K., Reda, S., Finke, C., Graul-Neumann, L., Jost-Brinkmann, P., & Bartzela, T. (2017). Oral manifestations, dental management, and a rare homozygous mutation of the PRDM12 gene in a boy with hereditary sensory and autonomic neuropathy type VIII: A case report and review of the literature. BMC.

Chicago Style (17th ed.) Citation

Elhennawy, Karim, Seif Reda, Christian Finke, Luitgard Graul-Neumann, Paul-Georg Jost-Brinkmann, and Theodosia Bartzela. Oral Manifestations, Dental Management, and a Rare Homozygous Mutation of the PRDM12 Gene in a Boy with Hereditary Sensory and Autonomic Neuropathy Type VIII: A Case Report and Review of the Literature. BMC, 2017.

MLA (8th ed.) Citation

Elhennawy, Karim, et al. Oral Manifestations, Dental Management, and a Rare Homozygous Mutation of the PRDM12 Gene in a Boy with Hereditary Sensory and Autonomic Neuropathy Type VIII: A Case Report and Review of the Literature. BMC, 2017.