AKBARIAZAR, E.; EBRAHIMPOUR, M. R.; AKBARI, S.; ARZHANGHI, S.; ABEDINI, S. S.; NAJMABADI, H.; KAHRIZI, K. A novel deletion mutation in ASPM gene in an Iranian family with autosomal recessive primary microcephaly. Iranian Journal of Child Neurology, [S. l.], v. 7, n. 2, p. 23–30, 2013. DOI: 10.22037/ijcn.v7i2.3840. Disponível em: https://journals.sbmu.ac.ir/ijcn/article/view/3840. Acesso em: 2 may. 2024.