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Arch Iran Med. 2020;23(5): 319-325. doi: 10.34172/aim.2020.21

Original Article

Limbic System Associated Membrane Protein Mutation in an Iranian Family Diagnosed with Ménière’s Disease

Zohreh Mehrjoo 1 ORCID, Kimia Kahrizi 1, Marzieh Mohseni 1, Mojdeh Akbari 1, Sanaz Arzhangi 1, Khadijeh Jalalvand 1, Hossein Najmabadi 1, Mohammad Farhadi 2, Mohammad Mohseni 2, Alimohamad Asghari 3, Saleh Mohebbi 3, Ahmad Daneshi 2 * ORCID

Cited by CrossRef: 6


1- Parra-Perez A, Lopez-Escamez J. Types of Inheritance and Genes Associated with Familial Meniere Disease. JARO. 2023;24(3):269 [Crossref]
2- Escalera-Balsera A, Roman-Naranjo P, Lopez-Escamez J. Systematic Review of Sequencing Studies and Gene Expression Profiling in Familial Meniere Disease. Genes. 2020;11(12):1414 [Crossref]
3- Zhang S, Guo Z, Tian E, Liu D, Wang J, Kong W. Meniere disease subtyping: the direction of diagnosis and treatment in the future. Expert Review of Neurotherapeutics. 2022;22(2):115 [Crossref]
4- Upmale-Engela S, Vaivode I, Peculis R, Litvina H, Zake T, Skesters A, Gogins D, Rovite V, Konrade I. Genetic and Environmental Factors in Autoimmune Thyroid Disease: Exploring Associations with Selenium Levels and Novel Loci in a Latvian Cohort. CIMB. 2024;46(3):2553 [Crossref]
5- Garofalo M, Vansenne F, Sival D, Verbeek D. Pathogenetic Insights into Developmental Coordination Disorder Reveal Substantial Overlap with Movement Disorders. Brain Sciences. 2023;13(12):1625 [Crossref]
6- Dai Q, Long L, Zhao H, Wang R, Zheng H, Duan M. Genetic advances in Meniere Disease. Mol Biol Rep. 2023;50(3):2901 [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.