Next-generation sequencing identified novel truncating mutations in BBS9 causing Bardet Biedl syndrome in two Iranian consanguineous families

por AKBAROGHLI, Susan, KOOSHAVAR, Daniz, GOLCHEHRE, Zahra, KARAMZADE, Arezou, SABERI, Mohammad, ALAEI, Mohammad Reza, ABBASI SADEGH, Masoud, ASADOLLAHI, Mostafa, KERAMATIPOUR, Mohammad
Publicado 2022