Publications by authors named "Ata Bushehri"

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Identification of a Novel Homozygous Mutation in Gene in an Iranian Family with Bardet-Biedl Syndrome.
Mohammad Dehani, Davood Zare-Abdollahi, Ata Bushehri, Azadeh Dehghani, Jalil Effati

Avicenna J Med Biotechnol· January 2021

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Novel Bi-allelic PDE6C Variant Leads to Congenital Achromatopsia.
Ata Bushehri, Davood Zare-Abdollahi, Hesam Hashemian, Ladan Safavizadeh, Jalil Effati

Iran Biomed J· July 2020

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Bi-allelic Mutations in ALDH5A1 is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability.
Mahshid Fattahi, Ata Bushehri, Afagh Alavi, Vahid Asghariazar, Ahoura Nozari

Gene· July 2020

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RPE65 and retinal dystrophy: Report of new and recurrent mutations.
Shamsi Safari, Davood Zare-Abdollahi, Ata Bushehri, Mohammad Reza Safari, Azadeh Dehghani

J Gene Med· March 2020

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MFSD8 gene mutations; evidence for phenotypic heterogeneity.
Davood Zare-Abdollahi, Ata Bushehri, Afagh Alavi, Alireza Dehghani, Mohammadreza Mousavi-Mirkala

Ophthalmic Genet· April 2019

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Identification of PROS1 as a Novel Candidate Gene for Juvenile Retinitis Pigmentosa.
Ata Bushehri, Davood Zare-Abdollahi, Afagh Alavi, Alireza Dehghani, Mohammadreza Mousavimikala

Int J Mol Cell Med· January 2019

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