Identifying Effective Drivers in the Future of Sports Businesses in Khorasan Razavi Province von Mohammad Ali Sahebkaran, Jafar Khoshbakhti, Raheleh Kariminejad

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Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population von Abolhassani, Ayda, Fattahi, Zohreh, Beheshtian, Maryam, Fadaee, Mahsa, Vazehan, Raheleh, Ahangari, Fatemeh, Dehdahsi, Shima, Faraji Zonooz, Mehrshid, Parsimehr, Elham, Kalhor, Zahra, Peymani, Fatemeh, Mozaffarpour Nouri, Maryam, Babanejad, Mojgan, Noudehi, Khadijeh, Fatehi, Fatemeh, Zamanian Najafabadi, Shima, Afroozan, Fariba, Yazdan, Hilda, Bozorgmehr, Bita, Azarkeivan, Azita, Sadat Mahdavi, Shokouh, Nikuei, Pooneh, Fatehi, Farzad, Jamali, Payman, Ashrafi, Mahmoud Reza, Karimzadeh, Parvaneh, Habibi, Haleh, Kahrizi, Kimia, Nafissi, Shahriar, Kariminejad, Ariana, Najmabadi, Hossein

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P604: Diagnostic utility of NGS testing in a highly consanguineous population: Findings from 1400+ Iranian patients with Mendelian disorders von Abolhassani, Ayda, Fattahi, Zohreh, Beheshtian, Maryam, Fadaee, Mahsa, Vazehan, Raheleh, Ahangari, Fatemeh, Dehdahsi, Shima, Zonooz, Mehrshid Faraji, Parsimehr, Elham, Kalhor, Zahra, Peymani, Fatemeh, Nouri, Maryam Mozaffarpour, Babanejad, Mojgan, Noudehi, Khadijeh, Fatehi, Fatemeh, Najafabadi, Shima Zamanian, Afroozan, Fariba, Yazdan, Hilda, Bozorgmehr, Bita, Azarkeivan, Azita, Mahdavi, Shokouh Sadat, Nikuei, Pooneh, Fatehi, Farzad, Jamali, Payman, Ashrafi, Mahmoud Reza, Karimzadeh, Parvaneh, Habibi, Haleh, Kahrizi, Kimia, Nafissi, Shahriar, Kariminejad, Ariana, Najmabadi, Hossein

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Molecular Diagnosis of Hereditary Neuropathies by Whole Exome Sequencing and Expanding the Phenotype Spectrum von Taghizadeh, Sara, Vazehan, Raheleh, Beheshtian, Maryam, Sadeghinia, Farnaz, Fattahi, Zohreh, Mohseni, Marzieh, Arzhangi, Sanaz, Nafissi, Shahriar, Kariminejad, Ariana, Najmabadi, Hossein, Kahrizi, Kimia

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CEP104 and CEP290 ; Genes with Ciliary Functions Cause Intellectual Disability in Multiple Families von Khoshbakht, Shahrouz, Beheshtian, Maryam, Fattahi, Zohreh, Bazazzadegan, Niloofar, Parsimehr, Elham, Fadaee, Mahsa, Vazehan, Raheleh, Faraji Zonooz, Mehrshid, Abolhassani, Ayda, Makvand, Mina, Kariminejad, Ariana, Celik, Arzu, Kahrizi, Kimia, Najmabadi, Hossein

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Identification of disease‐causing variants in the EXOSC gene family underlying autosomal recessive intellectual disability in Iranian families von Beheshtian, Maryam, Fattahi, Zohreh, Fadaee, Mahsa, Vazehan, Raheleh, Jamali, Payman, Parsimehr, Elham, Kamgar, Mahboubeh, Zonooz, Mehrshid Faraji, Mahdavi, Shokouh Sadat, Kalhor, Zahra, Arzhangi, Sanaz, Abedini, Seyedeh Sedigheh, Kermani, Farahnaz Sabbagh, Mojahedi, Faezeh, Kalscheuer, Vera M., Ropers, Hans‐Hilger, Kariminejad, Ariana, Najmabadi, Hossein, Kahrizi, Kimia

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Report of limb girdle muscular dystrophy type 2a in 6 Iranian patients, one with a novel deletion in CAPN3 gene von Fadaee, Mahsa, Kariminejad, Ariana, Fattahi, Zohreh, Nafissi, Shahriar, Godarzi, Hamed Reza, Beheshtian, Maryam, Vazehan, Raheleh, Akbari, Mohammad Reza, Kahrizi, Kimia, Najmabadi, Hossein

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Brief Report of Variants Detected in Hereditary Hearing Loss Cases in Iran over a 3-Year Period von Bazazzadegan, Niloofar, Vazehan, Raheleh, Fadaee, Mahsa, Fattahi, Zohreh, Abolhassani, Ayda, Parsimehr, Elham, Kalhor, Zahra, Faraji Zonooz, Mehrshid, Ahangari, Fatemeh, Dehdahsi, Shima, Samiee, Farshide, Jamali, Payman, Habibi, Haleh, Nourizadeh, Younes, Mahdavi, Shokouh, Beheshtian, Maryam, Kariminejad, Ariana, Smith, Richard Jh, Najmabadi, Hossein

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De novo Mutation in CACNA1S Gene in a 20-Year-Old Man Diagnosed with Metabolic Myopathy von Edizadeh, Masoud, Vazehan, Raheleh, Javadi, Fatemeh, Shima Dehdahsi, Fadaee, Mahsa, Mehrshid Faraji Zonooz, Parsimehr, Elham, Ahangari, Fatemeh, Abolhassani, Ayda, Kalhor, Zahra, Fattahi, Zohreh, Beheshtian, Maryam, Kariminejad, Ariana, Akbari, Mohammad Reza, Najmabadi, Hossein, Nafissi, Shahriar

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