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

Zohreh Mehrjoo ¹ , 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 *

Cited by CrossRef: 4

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.