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Akbaroghli, S., Kooshavar, D., Golchehre, Z., Karamzade, A., Saberi, M., Alaei, M.R., Abbasi Sadegh, M., Asadollahi, M. and Keramatipour, M. 2022. 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. 16, 1 (Jan. 2022), 123–133. DOI:https://doi.org/10.22037/ijcn.v16i1.31650.