Akbaroghli, S., D. Kooshavar, Z. Golchehre, A. Karamzade, M. Saberi, M. R. Alaei, M. Abbasi Sadegh, M. Asadollahi, and M. Keramatipour. “Next Generation Sequencing Identified Novel Truncating Mutations in BBS9 Causing Bardet Biedl Syndrome in Two Iranian Consanguineous Families: Two Novel Pathogenic Variants in BBS9 Gene”. Iranian Journal of Child Neurology, vol. 16, no. 1, Jan. 2022, pp. 123-3, doi:10.22037/ijcn.v16i1.31650.