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Pourahmadiyan, A and Alipour, P and Fattahi, N and Kasiri, M and Rezaeian, F and Taghipour-Sheshdeh A, A and Mohammadi-Asl, J and Tabatabaiefar, M and Hashemzadeh Chaleshtori, M (2019) A pathogenic variant in SLC26A4 is associated with Pendred syndrome in a consanguineous Iranian family. Int J Audiol.