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
Fatemeh Azadegan-Dehkordi, Tayyebe Bahrami, Maryam Shirzad, Gelareh Karbasi, Nasrin Yazdanpanahi, Effat Farrokhi, Mahbobeh Koohiyan, Mohammad Amin Tabatabaiefar, Morteza Hashemzadeh-Chaleshtori
J Audiol Otol. 2019;23(1):20-26.   Published online 2018 Dec 7     DOI: https://doi.org/10.7874/jao.2018.00185
Citations to this article as recorded by Crossref logo
Molecular diagnosis of SLC26A4-related hereditary hearing loss in a group of patients from two provinces of Iran
Mahbobeh Koohiyan, Morteza Hashemzadeh-Chaleshtori, Mohammad Amin Tabatabaiefar
Intractable & Rare Diseases Research.2021; 10(1): 23.     CrossRef
Rare mutations in Atoh1 lead to hearing loss
Samira Ajdari, Javad Saffari-Chaleshtori, Zahra Pourteymourfard-Tabrizi, Payam Ghasemi-Dehkordi, Mahdi Ghatreh Samani, Majid Validi, Hamidreza Kabiri, Morteza Hashemzadeh Chaleshtori, Mohammad-Saeid Jami
Gene Reports.2021; 24: 101254.     CrossRef
GJB2 ‐related hearing loss in central Iran: Review of the spectrum and frequency of gene mutations
Mahbobeh Koohiyan, Farideh Koohian, Fatemeh Azadegan‐Dehkordi
Annals of Human Genetics.2020; 84(2): 107.     CrossRef
Next generation sequencing and genetics of hereditary hearing loss in the iranian population: New insights from a systematic review
Mahbobeh koohiyan
International Journal of Pediatric Otorhinolaryngology.2020; 129: 109756.     CrossRef
Identification and clinical implications of a novel pathogenic variant in the GJB2 gene causes autosomal recessive non-syndromic hearing loss in a consanguineous Iranian family
Mahbobeh Koohiyan
Intractable & Rare Diseases Research.2020; 9(1): 30.     CrossRef
Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden
Samuel Mawuli Adadey, Edmond Wonkam-Tingang, Elvis Twumasi Aboagye, Daniel Wonder Nayo-Gyan, Maame Boatemaa Ansong, Osbourne Quaye, Gordon A. Awandare, Ambroise Wonkam
Life.2020; 10(11): 258.     CrossRef
An update of spectrum and frequency of GJB2 mutations causing hearing loss in the south of Iran: A literature review
Mahbobeh koohiyan, Amirhossein Ahmadi, Farideh koohian, Shahrzad Aghaei, Beheshteh Amiri, Morteza Hashemzadeh-Chaleshtori
International Journal of Pediatric Otorhinolaryngology.2019; 119: 136.     CrossRef
A systematic review of SLC26A4 mutations causing hearing loss in the Iranian population
Mahbobeh koohiyan
International Journal of Pediatric Otorhinolaryngology.2019; 125: 1.     CrossRef
Genetics of hereditary hearing loss in east Iran population: A systematic review of GJB2 mutations
Mahbobeh Koohiyan, Fatemeh Azadegan-Dehkordi, Farideh Koohian, Marziye Abolhasani, Morteza Hashemzadeh-Chaleshtori
Intractable & Rare Diseases Research.2019; 8(3): 172.     CrossRef
Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations
Mahbobeh Koohiyan, Fatemeh Azadegan-Dehkordi, Farideh Koohian, Morteza Hashemzadeh-Chaleshtori
Journal of Audiology and Otology.2019; 23(4): 175.     CrossRef