Search Results - Samira Behroozi

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    A novel recessive PDZD7 bi-allelic mutation in an Iranian family with non-syndromic hearing loss by Hossein Fahimi, Samira Behroozi, Sadaf Noavar, Farshid Parvini

    Published 2021
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    A novel homozygous frame-shift mutation in the SLC29A3 gene: a new case report and review of literature by Sadaf Noavar, Samira Behroozi, Taraneh Tatarcheh, Farshid Parvini, Majid Foroutan, Hossein Fahimi

    Published 2019
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