An Iranian familial amyotrophic lateral sclerosis pedigree with p.Val48Phe causing mutation in SOD1: a genetic and clinical report by Afagh Alavi, Marzieh Khani, Shahriar Nafissi, Hosein Shamshiri, Elahe Elahi

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Intellectual disability associated with craniofacial dysmorphism due to POLR3B mutation and defect in spliceosomal machinery by Mostafa Saghi, Kolsoum InanlooRahatloo, Afagh Alavi, Kimia Kahrizi, Hossein Najmabadi

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A novel nonsense mutation in WNK1/HSN2 associated with sensory neuropathy and limb destruction in four siblings of a large Iranian pedigree by Behrouz Rahmani, Fatemeh Fekrmandi, Keivan Ahadi, Tannaz Ahadi, Afagh Alavi, Abolhassan Ahmadiani, Sareh Asadi

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A Pathogenic Homozygous Mutation In The Pleckstrin Homology Domain Of RASA1 Is Responsible For Familial Tricuspid Atresia In An Iranian Consanguineous Family by Ahoura Nozari, Ehsan Aghaei-Moghadam, Aliakbar Zeinaloo, Afagh Alavi, Saghar Ghasemi Firouzabad, Shohre Minaee, Marzeieh Eskandari Hesari, Farkhondeh Behjati

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Potential role of FKBP5 single‐nucleotide polymorphisms in functional seizures by Ali A. Asadi‐Pooya, Leila Simani, Marjan Asadollahi, Fatemeh Sadat Rashidi, Ehsan Ahmadipour, Afagh Alavi, Mehrdad Roozbeh, Nayyereh Akbari, Negar Firouzabadi

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Description of combined ARHSP/JALS phenotype in some patients with SPG11 mutations by Marzieh Khani, Hosein Shamshiri, Farzad Fatehi, Mohammad Rohani, Bahram Haghi Ashtiani, Fahimeh Haji Akhoundi, Afagh Alavi, Hamidreza Moazzeni, Hanieh Taheri, Mina Tolou Ghani, Leila Javanparast, Seyyed Saleh Hashemi, Ramona Haji‐Seyed‐Javadi, Matineh Heidari, Shahriar Nafissi, Elahe Elahi

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