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Arch Iran Med. 2022;25(12): 788-797. doi: 10.34172/aim.2022.124
PMID: 37543906        PMCID: PMC10685845

Original Article

Characterizing Genotypes and Phenotypes Associated with Dysfunction of Channel-Encoding Genes in a Cohort of Patients with Intellectual Disability

Naeim Ehtesham 1 ORCID, Meysam Mosallaei 1, Maryam Beheshtian 1 ORCID, Shahrouz Khoshbakht 1, Mahsa Fadaee 2, Raheleh Vazehan 2, Mehrshid Faraji Zonooz 2, Parvaneh Karimzadeh 3 ORCID, Kimia Kahrizi 1, Hossein Najmabadi 1,2 * ORCID

Cited by CrossRef: 1

1- Cipriano L, Piscopo R, Aiello C, Novelli A, Iolascon A, Piscopo C. Expanding the Phenotype of the CACNA1C-Associated Neurological Disorders in Children: Systematic Literature Review and Description of a Novel Mutation. Children. 2024;11(5):541 [Crossref]

SCImago Journal & Country Rank

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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.