Items where Author is "Mirfakhraie, R."
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Number of items: 3.
(2021) Targeted sequencing of CDH23 and GJB2 genes in an Iranian pedigree with Usher syndrome and non-syndromic hearing loss. Gene Reports.
(2021) Whole exome sequencing identified a novel homozygous ARV1 mutation in an Iranian family with developmental and epileptic encephalopathy-38. META GENE. ISSN 2214-5400 J9 - META GENE
(2017) Evaluation of promoter methylation status of MLH1 gene in Iranian patients with colorectal tumors and adenoma polyps. Gastroenterology and hepatology from bed to bench. S117-S121. ISSN 2008-2258 (Print) 2008-2258 (Linking)