Rafat Noeiaghdam
2PUBLICATIONS
5CO-AUTHORS
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Publications (2)
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|Nov 28, 2022
A rare case of SRD5A3-CDG in a patient with ataxia and telangiectasia: A case report.Sayyed Hesamedin Nabavizadeh, Rafat Noeiaghdam, Leila Johari
|Oct 10, 2022
Homozygous Autosomal Recessive DIAPH1 Mutation Associated with Central Nervous System Involvement and Aspergillosis: A Rare Case.Hossein Esmaeilzadeh, Rafat Noeiaghdam, Leila Johari
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