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

Shahrouz Khoshbakht ¹, Maryam Beheshtian ^1,2, Zohreh Fattahi ^1,2, Niloofar Bazazzadegan ¹, Elham Parsimehr ², Mahsa Fadaee ², Raheleh Vazehan ², Mehrshid Faraji Zonooz ², Ayda Abolhassani ², Mina Makvand ², Ariana Kariminejad ², Arzu Celik ³, Kimia Kahrizi ¹, Hossein Najmabadi ^1,2 *

Cited by CrossRef: 1

1- Badv R, Mahdiannasser M, Rasoulinezhad M, Habibi L, Rashidi-Nezhad A. CEP104 gene may involve in the pathogenesis of a new developmental disorder other than joubert syndrome. Mol Biol Rep. 2022;49(8):7231 [Crossref]

2- Lyu T, Ma J, Zhang X, Xie G, Liu C, Du J, Xu Y, Yang D, Cen C, Wang M, Lyu N, Wang Y, Zhang H. Deficiency of FRMD5 results in neurodevelopmental dysfunction and autistic-like behavior in mice. Mol Psychiatry. 2024; [Crossref]

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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.