- Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations
-
Koohiyan M, Azadegan-Dehkordi F, Koohian F, Hashemzadeh-Chaleshtori M
- KMID: 2460017
- J Audiol Otol.
- 2019 Oct;23(4):175-180.
- doi: 10.7874/jao.2019.00059
Diagnosis of pre-lingual hearing loss (HL) is difficult owing to the high number of genes responsible. The most frequent cause of HL is DFNB1 due to mutations in the GJB2... -
- CITED
-
- Close
- SHARE
-
- Close
- MicroRNA-183 Family in Inner Ear: Hair Cell Development and Deafness
-
Mahmoodian sani MR, Hashemzadeh-Chaleshtori M, Saidijam M, Jami MS, Ghasemi-Dehkordi P, Saidijam M, Jami MS
- KMID: 2361685
- J Audiol Otol.
- 2016 Dec;20(3):131-138.
- doi: 10.7874/jao.2016.20.3.131
miRNAs are essential factors of an extensively conserved post-transcriptional process controlling gene expression at mRNA level. Varoius biological processes such as growth and differentiation are regulated by miRNAs. Web of... -
- CITED
-
- Close
- SHARE
-
- Close
- Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran
-
Azadegan-Dehkordi F, Bahrami T, Shirzad M, Karbasi G, Yazdanpanahi N, Farrokhi E, Koohiyan M, Tabatabaiefar MA, Hashemzadeh-Chaleshtori M
- KMID: 2438178
- J Audiol Otol.
- 2019 Jan;23(1):20-26.
- doi: 10.7874/jao.2018.00185
BACKGROUND AND OBJECTIVES: Autosomal recessive non-syndromic hearing loss (ARNSHL) with genetic origin is common (1/2000 births). ARNSHL can be associated with mutations in gap junction protein beta 2 (GJB2). To... -
- CITED
-
- Close
- SHARE
-
- Close
