AKBAROGHLI, S.; KOOSHAVAR, D.; GOLCHEHRE, Z.; KARAMZADE, A.; SABERI, M.; ALAEI, M. R.; ABBASI SADEGH, M.; ASADOLLAHI, M.; KERAMATIPOUR, M. 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, [S. l.], v. 16, n. 1, p. 123–133, 2022. DOI: 10.22037/ijcn.v16i1.31650. Disponível em: https://journals.sbmu.ac.ir/ijcn/article/view/31650. Acesso em: 19 may. 2024.