Mutation screening of exons 7 and 13 of the TMC1 gene in autosomal recessive non-syndromic hearing loss (ARNSHL) in Iran
By: Moradipour, Negar; Heibati, Fatimah; Abu al-Husni, Marziyah…[et al.]. Iranian Red Crescent Medical Journal. Vol. 18, no. 3 (Mar. 2016), pp.1-6, 6 p.
Subjects: Deafness; Iran; Genetic aspects