Adnan Issa Al-Badran
2PUBLICATIONS
6CO-AUTHORS

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Publications (2)
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|Oct 24, 2024
Identification and characterization of NMNAT1 gene mutations in an Iranian patient with Leber congenital amaurosis 9.Mostafa Neissi, Motahareh Sheikh-Hosseini, Misagh Mohammadi-Asl
|Aug 18, 2024
Usher Syndrome Type 2 in An Iranian Family: A Novel Founder Variation in The USH2A Gene.Mostafa Neissi, Javad Mohammadi-Asl, Misagh Mohammadi-Asl
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