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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