1. De novo Mutation in CACNA1S Gene in a 20-Year-Old Man Diagnosed with Metabolic Myopathy

Masoud Edizadeh, Raheleh Vazehan, Fatemeh Javadi, Shima Dehdahsi, Mahsa Fadaee, Mehrshid Faraji Zonooz, Elham Parsimehr, Fatemeh Ahangari, Ayda Abolhassani, Zahra Kalhor, Zohreh Fattahi, Maryam Beheshtian, Ariana Kariminejad, Mohammad Reza Akbari, Hossein Najmabadi*, Shahriar Nafissi*

Arch Iran Med. 2017;20(9): .

PMID: 29048924 Scopus ID: 85032364708

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2. CEP104 and CEP290; Genes with Ciliary Functions Cause Intellectual Disability in Multiple Families

Shahrouz Khoshbakht, Maryam Beheshtian, Zohreh Fattahi, Niloofar Bazazzadegan, Elham Parsimehr, Mahsa Fadaee, Raheleh Vazehan, Mehrshid Faraji Zonooz, Ayda Abolhassani, Mina Makvand, Ariana Kariminejad, Arzu Celik, Kimia Kahrizi, Hossein Najmabadi*

Arch Iran Med. 2021;24(5): 364-373. doi: 10.34172/aim.2021.53

Scopus ID: 85108797588

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A Monthly Peer-Reviewed Medical Journal Published by the Academy of Medical Sciences of the I.R. Iran; Indexed in PubMed/MEDLINE, ISI Web of Science, EMBASE, SCOPUS, CINHAL, PASCAL, CSA, SID, ISSN: Print 1029-2977, Online 1735-3947.The impact factor of Archives of Iranian Medicine according to Journal Citation Reports® (JCR®) 2016 is 1.20.