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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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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