APA Citatie

Santoro, C., Giugliano, T., Bernardo, P., Palladino, F., Torella, A., del Vecchio Blanco, F., . . . Piluso, G. (2020). A novel RAB39B mutation and concurrent de novo NF1 mutation in a boy with neurofibromatosis type 1, intellectual disability, and autism: A case report. BMC Neurol.

Chicago Style citaat

Santoro, Claudia, et al. "A Novel RAB39B Mutation and Concurrent De Novo NF1 Mutation in a Boy With Neurofibromatosis Type 1, Intellectual Disability, and Autism: A Case Report." BMC Neurol 2020.

MLA citatie

Santoro, Claudia, et al. "A Novel RAB39B Mutation and Concurrent De Novo NF1 Mutation in a Boy With Neurofibromatosis Type 1, Intellectual Disability, and Autism: A Case Report." BMC Neurol 2020.