Sepideh Rezakhani
2PUBLICATIONS
0CO-AUTHORS
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Publications (2)
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|Nov 18, 2022
Developmental regression and movement disorder as a phenotypic variant of POLR3A Mutation-Case report.Ali Nikkhah, Sepideh Rezakhani
|Aug 08, 2022
Neurodegenerative disorder and diffuse brain calcifications due to FARSB mutation in two siblings.Parvaneh Karimzadeh, Sepideh Rezakhani, Mohammad Miryounesi
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