Mohammad Amin Tabatabaiefar

2PUBLICATIONS
2CO-AUTHORS
Neurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)
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Publications (2)

|Jul 06, 2020
Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss.

Akram Sarmadi, Samane Nasrniya, Sina Narrei

|Sep 13, 2019
GJB2-related hearing loss in central Iran: Review of the spectrum and frequency of gene mutations.

Mahbobeh Koohiyan, Farideh Koohian, Fatemeh Azadegan-Dehkordi

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Frequent Collaborators

1 joint publications

Farideh Koohian

1 joint publications

Fatemeh Azadegan-Dehkordi