Publications by authors named "Seyyed Mohammad Lesani"
Investigation of LRTOMT gene (locus DFNB63) mutations in Iranian patients with autosomal recessive non-syndromic hearing loss.
Seyyed Hossein Taghizadeh Seyyed Reza Kazeminezhad Seyyed Ali Asghar Sefidgar Nasrin Yazdanpanahi Mohammad Amin Tabatabaeifar Seyyed Mohammad Lesani
Int J Mol Cell Med
February 2014
Hearing loss (HL) is the most frequent sensory defect affecting 1 in 1000 neonates. This can occur due to genetic or environmental causes or both. The genetic causes are very heterogenous and over 100 loci have been identified to cause autosomal recessive non - syndromic hearing loss (ARNSHL).
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