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
Crossref DOI link: https://doi.org/10.1186/s13256-017-1387-z
Published Online: 2017-08-15
Published Print: 2017-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Elhennawy, Karim
Reda, Seif
Finke, Christian
Graul-Neumann, Luitgard
Jost-Brinkmann, Paul-Georg
Bartzela, Theodosia