SALEHPOUR, S., HASHEMI-GORJI, F., SOLTANI, Z., GHAFOURI-FARD, S. and MIRYOUNESI, M. (2017) “Association of a Novel Nonsense Mutation in KIAA1279 with Goldberg-Shprintzen Syndrome”, Iranian Journal of Child Neurology, 11(1), pp. 70–74. doi: 10.22037/ijcn.v11i1.12498.