Items where Author is "Taghipour-Sheshdeh, A."

Article

(2019) Identification and Clinical Implications of a Novel MYO15A Variant in a Consanguineous Iranian Family by Targeted Exome Sequencing. Audiology and Neuro-Otology. pp. 25-31. ISSN 1420-3030

(2019) A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family. Genomics. pp. 840-848. ISSN 0888-7543

(2019) A pathogenic variant in SLC26A4 is associated with Pendred syndrome in a consanguineous Iranian family. Int J Audiol. pp. 1-7. ISSN 1708-8186 (Electronic) 1499-2027 (Linking)

(2018) A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family. Genomics. ISSN 1089-8646 (Electronic) 0888-7543 (Linking)