Unraveling the Genetic Landscape of Hearing Loss: A Comprehensive Study of Azeri Families in Ardabil, Iran by Marzieh Mohseni, Farzane Zare Ashrafi, Ehsan Abbaspour Rodbaneh, Haleh Mokabber, Maryam Vafaei, Ramiz Nobakht, Fatemeh Keshavarzi, Sanaz Arzhangi, Sara Arish, Zahra Nematollahi Azar, Kimia Kahrizi, Hossein Najmabadi, Behzad Davarnia

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A mutation causes MuSK reduced sensitivity to agrin and congenital myasthenia. by Asma Ben Ammar, Payam Soltanzadeh, Stéphanie Bauché, Pascale Richard, Evelyne Goillot, Ruth Herbst, Karen Gaudon, Caroline Huzé, Laurent Schaeffer, Yuji Yamanashi, Osamu Higuchi, Antoine Taly, Jeanine Koenig, Jean-Paul Leroy, Fayçal Hentati, Hossein Najmabadi, Kimia Kahrizi, Manouchehr Ilkhani, Michel Fardeau, Bruno Eymard, Daniel Hantaï

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BOD1 Is Required for Cognitive Function in Humans and Drosophila. by Sahar Esmaeeli-Nieh, Michaela Fenckova, Iain M Porter, M Mahdi Motazacker, Bonnie Nijhof, Anna Castells-Nobau, Zoltan Asztalos, Robert Weißmann, Farkhondeh Behjati, Andreas Tzschach, Ute Felbor, Harry Scherthan, Seyed Morteza Sayfati, H Hilger Ropers, Kimia Kahrizi, Hossein Najmabadi, Jason R Swedlow, Annette Schenck, Andreas W Kuss

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CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival by Vincent Michel, Kevin T Booth, Pranav Patni, Matteo Cortese, Hela Azaiez, Amel Bahloul, Kimia Kahrizi, Ménélik Labbé, Alice Emptoz, Andrea Lelli, Julie Dégardin, Typhaine Dupont, Asadollah Aghaie, Danuta Oficjalska‐Pham, Serge Picaud, Hossein Najmabadi, Richard J Smith, Michael R Bowl, Steven DM Brown, Paul Avan, Christine Petit, Aziz El‐Amraoui

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P251: New insights into the genetic landscape of DMD gene mutations in Iran and the applicability of exon skipping therapies by Ali Khanbazi, Farzane Zare Ashrafi, Masoumeh Akbari Kelishomi, Raziye Rezvani Rezvandeh, Maryam Azad, Fatemeh Ahangari, Mahsa Fadaee, Shima Dehdahsi, Mina Makvand, Banafsheh Salmani, Zohreh Vahidi, Mahdieh Kooshki, Elmira Shiuokhi, Armita Ghaderi, Mahsa Tahmasebivand, Fariba Afroozan, Khadijeh Noudehi, Fatemeh Fatehi, Shima Zamanian Najafabadi, Shahriar Nafissi, Haleh Habibi, Maryam Taghdiri, Bahram Haghi Ashtiani, Gholamreza Zamani, Fatemeh Mohsenifar, Farzad Fatehi, MohammadKazem Bakhshandeh, Payman Jamali, Kimia Kahrizi, Ariana Kariminejad, Hossein Najmabadi

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P279: Application of next-generation sequencing in the diagnosis of inherited metabolic disorders in Iran: An 11-year overview by Parnian Alagha, Negar Molaei, Maryam Beheshtian, Fatemeh Ahangari, Mahsa Fadaee, Mehri Ashki, Zohreh Elahi, Raheleh Vazehan, Shima Dehdahsi, Elham Parsimehr, Maryam Mozaffarpour Nouri, Parishad Saei, Khadijeh Noudehi, Fatemeh Fatehi, Shima Zamanian Najafabadi, Hilda Yazdan, Fariba Afroozan, Banafsheh Salmani, Mahdieh Kooshki, Armita Ghaderi, Zohreh Vahidi, Mina Makvand, Atiyeh Ahmadpour, Mahsa Tahmasebivand, Elmira Shiuokhi, Saeed Talebi, Babak Zamani, Farhad Mahvelati Shamsabadi, Bahram Haghi Ashtiani, Payam Sarraf, Haleh Habibi, Afshin Fayyazi, Ali Asghar Okhovat, Mahmoud Reza Ashrafi, Farzad Fatehi, Parvaneh Karimzadeh, Shahriar Nafissi, Kimia Kahrizi, Ariana Kariminejad, Hossein Najmabadi

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P159: Gene and mutation spectrum among Iranian individuals with neuromuscular disorders: An 11-year consolidated overview* by Negar Molaei, Parnian Alagha, Ali Khanbazi, Maryam Beheshtian, Fatemeh Ahangari, Mahsa Fadaee, Mehri Ashki, Zohreh Elahi, Raheleh Vazehan, Shima Dehdahsi, Elham Parsimehr, Maryam Mozaffarpour Nouri, Parishad Saei, Khadijeh Noudehi, Fatemeh Fatehi, Shima Zamanian Najafabadi, Fariba Afroozan, Hilda Yazdan, Fariba Afroozan, Masoumeh Akbari Kelishomi, Maryam Azad, Seyed Mehrdad Kassaee, Mahtab Ramezani, Fariba Zemorshidi, Houman Salimipour, Siamak Abdi, MohammadKazem Bakhshandeh, Afshin Fayyazi, Gholamreza Zamani, Mahmoud Reza Ashrafi, Parvaneh Karimzadeh, Payman Jamali, Payam Sarraf, Ali Asghar Okhovat, Bahram Haghi Ashtiani, Farzad Fatehi, Shahriar Nafissi, Kimia Kahrizi, Ariana Kariminejad, Hossein Najmabadi

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