1. Sadeghi, Zahra, Chavoshi Tarzjani, Seyedeh Parisa, Miri Moosavi, Reyhaneh Sadat, Saber, Siamak, Ebrahimi, Ahmad. 2020. A Rare Mutation in the MARVELD2 Gene Can Cause Nonsyndromic Hearing Loss. In International medical case reports journal, 13, 291-296. doi:10.2147/IMCRJ.S257654. https://pubmed.ncbi.nlm.nih.gov/32884365/
2. Taghipour-Sheshdeh, Afsaneh, Nemati-Zargaran, Fatemeh, Zarepour, Narges, Mohammadi-Asl, Javad, Hashemzadeh-Chaleshtori, Morteza. 2018. A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family. In Genomics, 111, 840-848. doi:10.1016/j.ygeno.2018.05.008. https://pubmed.ncbi.nlm.nih.gov/29752989/
3. Zheng, Jing, Meng, Wen-Fang, Zhang, Chao-Fan, Chen, Ye, Guan, Min-Xin. 2018. New SNP variants of MARVELD2 (DFNB49) associated with non-syndromic hearing loss in Chinese population. In Journal of Zhejiang University. Science. B, 20, 164-169. doi:10.1631/jzus.B1700185. https://pubmed.ncbi.nlm.nih.gov/30406641/
4. Huang, Chuican, Huang, Zhenning, Wang, Ping, Fan, Xialin, Fan, Lichun. 2024. Case report: A novel nonsense mutation in the MARVELD2 gene causes nonsyndromic hearing loss in a China family. In Frontiers in genetics, 15, 1507600. doi:10.3389/fgene.2024.1507600. https://pubmed.ncbi.nlm.nih.gov/39698467/
5. Mašindová, Ivica, Šoltýsová, Andrea, Varga, Lukáš, Kádasi, Ľudevít, Gašperíková, Daniela. 2015. MARVELD2 (DFNB49) mutations in the hearing impaired Central European Roma population--prevalence, clinical impact and the common origin. In PloS one, 10, e0124232. doi:10.1371/journal.pone.0124232. https://pubmed.ncbi.nlm.nih.gov/25885414/
6. Šafka Brožková, D, Laštůvková, J, Štěpánková, H, Myška, P, Seeman, P. 2011. DFNB49 is an important cause of non-syndromic deafness in Czech Roma patients but not in the general Czech population. In Clinical genetics, 82, 579-82. doi:10.1111/j.1399-0004.2011.01817.x. https://pubmed.ncbi.nlm.nih.gov/22097895/
7. Shadab, Madiha, Abbasi, Ansar Ahmed, Ejaz, Ahsan, Kim, Hyung-Goo, Vona, Barbara. . Autosomal recessive non-syndromic hearing loss genes in Pakistan during the previous three decades. In Journal of cellular and molecular medicine, 28, e18119. doi:10.1111/jcmm.18119. https://pubmed.ncbi.nlm.nih.gov/38534090/
8. Mariano, Cibelle, Sasaki, Hiroyuki, Brites, Dora, Brito, Maria Alexandra. 2011. A look at tricellulin and its role in tight junction formation and maintenance. In European journal of cell biology, 90, 787-96. doi:10.1016/j.ejcb.2011.06.005. https://pubmed.ncbi.nlm.nih.gov/21868126/
9. Aliazami, Farnoush, Gilani, Sapideh, Farhud, Dariush, Afshari, Mahdi, Eslami, Maryam. 2023. Epidemiology, etiology, genetic variants in non- syndromic hearing loss in Iran: A systematic review and meta-analysis. In International journal of pediatric otorhinolaryngology, 168, 111512. doi:10.1016/j.ijporl.2023.111512. https://pubmed.ncbi.nlm.nih.gov/37086676/