Identification and characterization of NMNAT1 gene mutations in an Iranian patient with Leber congenital amaurosis 9 von Neissi, Mostafa, Sheikh‐Hosseini, Motahareh, Mohammadi‐Asl, Misagh, Al‐Badran, Adnan Issa, Roghani, Mojdeh, Mohammadi‐Asl, Javad, Jorfi, Kamele

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Usher Syndrome Type 2 in An Iranian Family: A Novel Founder Variation in The USH2A Gene von Neissi, Mostafa, Mohammadi-Asl, Javad, Mohammadi-Asl, Misagh, Roghani, Mojdeh, Sheikh-Hosseini, Motahareh, Issa Al-Badran, Adnan

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Comparison of the effects of olsalazine and decitabine on the expression of CDH1 and uPA genes and cytotoxicity in MDA-MB-231 breast cancer cells von Asl, Misagh, Asl, Javad, Naghitorabi, Mojgan

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Joubert syndrome caused by a TMEM67 mutation: Genotype-phenotype analysis von Neissi, Mostafa, Misagh Mohammadi-Asl, Mojdeh Roghani, Issa Al-Badran, Adnan, Motahareh Sheikh-Hosseini, Mohammadi-Asl, Javad

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Unveiling a Novel THOC2 Mutation's Role in X-linked Intellectual Disability von Mehdi Hashemipour, Ayad Neissi, Mostafa Neissi, Misagh Mohammadi-Asl, Motahareh Sheikh-Hosseini, Sasan Bavi, Mojdeh Roghani, Javad Mohammadi-Asl

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Mutation Detection in MYO15A Gene in an Iranian Family with Non-Syndromic Hearing Loss von Mostafa Neissi, Mostafa Neissi, Mohammadi-Asl, Misagh, Roghani, Mojdeh, Al-Badran, Adnan, Mohammadi-Asl, Javad

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Clinical and genetic analysis of Niemann-Pick disease type C with a novel NPC1 variant von Neissi, Mostafa, Al-Badran, Adnan Issa, Mohammadi-Asl, Misagh, Al-Badran, Raed Abdulelah, Sheikh-Hosseini, Motahareh, Roghani, Mojdeh, Mohammadi-Asl, Javad

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