Search filters

List of works by Effat Farrokhi

A 1 bp deletion in the dual reading frame deafness gene LRTOMT causes a frameshift from the first into the second reading frame.

scientific article

Compound Heterozygosity for Two Novel SLC26A4 Mutations in a Large Iranian Pedigree with Pendred Syndrome

scientific article

DFNB93, a novel locus for autosomal recessive moderate-to-severe hearing impairment.

scientific article published in June 2011

Digenic inheritance in autosomal recessive non-syndromic hearing loss cases carrying GJB2 heterozygote mutations: assessment of GJB4, GJA1, and GJC3.

scientific article published on 8 November 2012

Large-scale screening of mitochondrial DNA mutations among Iranian patients with prelingual nonsyndromic hearing impairment.

scientific article published on 11 November 2011

Molecular characterization of Iranian patients with possible familial hypercholesterolemia

scientific article

Oxidized low-density lipoprotein and upregulated expression of osteonectin and bone sialoprotein in vascular smooth muscle cells.

scientific article

Oxidized low-density lipoprotein increases bone sialoprotein expression in vascular smooth muscle cells via runt-related transcription factor 2.

scientific article published in March 2015

The role and spectrum of SLC26A4 mutations in Iranian patients with autosomal recessive hereditary deafness

scientific article published on 7 October 2014

Paulina is supported by:

About Paulina

Help