[1]
AKBARIAZAR, E., EBRAHIMPOUR, M.R., AKBARI, S., ARZHANGHI, S., ABEDINI, S.S., NAJMABADI, H. and KAHRIZI, K. 2013. A novel deletion mutation in ASPM gene in an Iranian family with autosomal recessive primary microcephaly. Iranian Journal of Child Neurology. 7, 2 (Apr. 2013), 23–30. DOI:https://doi.org/10.22037/ijcn.v7i2.3840.