Has participated in:
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Molecular Characterization of Genes Involved in Hearing Loss
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Hereditary hearing loss SNP-microarray pilot study
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A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans
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The conserved p.Arg108 residue in S1PR2 (DFNB68) is fundamental for proper hearing: evidence from a consanguineous Iranian family