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Najmeh Fattahi
Najmeh Fattahi
Shahrekord University of Medical Sciences
Biology
Mutation
Genetics
Gene
Hearing loss
6
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6
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0
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Differentiation of Mesenchymal Stem Cells into Photoreceptor-like Cells under the Influence of a Temporary Increase in miRNA-182, -183 Expression
2021
Mohammad-Reza Mahmoudian-Sani
Najmeh Fattahi
Samaneh Arab
Samira Asgharzade
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Molecular genetic study of glutaric aciduria, type I: Identification of a novel mutation: SHADMEHRI et al.
2019
Journal of Cellular Biochemistry
Azam Ahmadi Shadmehri
Najmeh Fattahi
Mohammad Reza Pourreza
Mahboobeh Koohiyan
Shahnaz Zarifi
Mojtaba Darbouy
Reza Sharifi
Javad Tavakkoly-Bazzaz
Mohammad Amin Tabatabaiefar
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A pathogenic variant in SLC26A4 is associated with Pendred syndrome in a consanguineous Iranian family
2019
International Journal of Audiology
Azam. Pourahmadiyan
Paria. Alipour
Najmeh Fattahi
Mahbubeh Kasiri
Fateme Rezaeian
Afsaneh Taghipour-Sheshdeh
Javad Mohammadi Asl
Mohammad Amin Tabatabaiefar
Morteza Hashemzadeh Chaleshtori
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Genetic linkage analysis of DFNB7/11 locus in patients with autosomal recessive non syndromic hearing loss from Hamedan province
2016
Journal of Shahrekord University of Medical Sciences
Azam Pourahmadiyam
Mohammad Amin Tabatabaefar
Somayeh. Reiisi
Pariya Alipour
Najmeh Fattahi
Morteza Hashemzadeh Chaleshtori
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