These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
22. Autosomal recessive nonsyndromic deafness genes: a review. Duman D; Tekin M Front Biosci (Landmark Ed); 2012 Jun; 17(6):2213-36. PubMed ID: 22652773 [TBL] [Abstract][Full Text] [Related]
23. Targeted Mutation Analysis of the SLC26A4, MYO6, PJVK and CDH23 Genes in Iranian Patients with AR Nonsyndromic Hearing Loss. Alimardani M; Hosseini SM; Khaniani MS; Haghi MR; Eslahi A; Farjami M; Chezgi J; Derakhshan SM; Mojarrad M Fetal Pediatr Pathol; 2019 Apr; 38(2):93-102. PubMed ID: 30582396 [TBL] [Abstract][Full Text] [Related]
24. Recurrent and private MYO15A mutations are associated with deafness in the Turkish population. Cengiz FB; Duman D; Sirmaci A; Tokgöz-Yilmaz S; Erbek S; Oztürkmen-Akay H; Incesulu A; Edwards YJ; Ozdag H; Liu XZ; Tekin M Genet Test Mol Biomarkers; 2010 Aug; 14(4):543-50. PubMed ID: 20642360 [TBL] [Abstract][Full Text] [Related]
25. GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants. Koohiyan M; Hashemzadeh-Chaleshtori M; Salehi M; Abtahi H; Reiisi S; Pourreza MR; Noori-Daloii MR; Tabatabaiefar MA Int J Pediatr Otorhinolaryngol; 2018 Apr; 107():121-126. PubMed ID: 29501291 [TBL] [Abstract][Full Text] [Related]
26. Expansion of phenotypic spectrum of MYO15A pathogenic variants to include postlingual onset of progressive partial deafness. Chang MY; Lee C; Han JH; Kim MY; Park HR; Kim N; Park WY; Oh DY; Choi BY BMC Med Genet; 2018 Feb; 19(1):29. PubMed ID: 29482514 [TBL] [Abstract][Full Text] [Related]
27. A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran. Babanejad M; Fattahi Z; Bazazzadegan N; Nishimura C; Meyer N; Nikzat N; Sohrabi E; Najmabadi A; Jamali P; Habibi F; Smith RJ; Kahrizi K; Najmabadi H Am J Med Genet A; 2012 Oct; 158A(10):2485-92. PubMed ID: 22903915 [TBL] [Abstract][Full Text] [Related]
28. Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families. Salime S; Charif M; Bousfiha A; Elrharchi S; Bakhchane A; Charoute H; Kabine M; Snoussi K; Lenaers G; Barakat A Int J Pediatr Otorhinolaryngol; 2017 Oct; 101():25-29. PubMed ID: 28964305 [TBL] [Abstract][Full Text] [Related]
29. Screening of the DFNB3 locus: identification of three novel mutations of MYO15A associated with hearing loss and further suggestion for two distinctive genes on this locus. Belguith H; Aifa-Hmani M; Dhouib H; Said MB; Mosrati MA; Lahmar I; Moalla J; Charfeddine I; Driss N; Arab SB; Ghorbel A; Ayadi H; Masmoudi S Genet Test Mol Biomarkers; 2009 Feb; 13(1):147-51. PubMed ID: 19309289 [TBL] [Abstract][Full Text] [Related]
30. Whole exome sequencing of six Chinese families with hereditary non-syndromic hearing loss. Liang P; Chen F; Wang S; Li Q; Li W; Wang J; Chen J; Zha D Int J Pediatr Otorhinolaryngol; 2021 Sep; 148():110817. PubMed ID: 34265623 [TBL] [Abstract][Full Text] [Related]
31. MYO15A splicing mutations in hearing loss: A review literature and report of a novel mutation. Motavaf M; Soveizi M; Maleki M; Mahdieh N Int J Pediatr Otorhinolaryngol; 2017 May; 96():35-38. PubMed ID: 28390610 [TBL] [Abstract][Full Text] [Related]
32. Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort. Bademci G; Foster J; Mahdieh N; Bonyadi M; Duman D; Cengiz FB; Menendez I; Diaz-Horta O; Shirkavand A; Zeinali S; Subasioglu A; Tokgoz-Yilmaz S; Huesca-Hernandez F; de la Luz Arenas-Sordo M; Dominguez-Aburto J; Hernandez-Zamora E; Montenegro P; Paredes R; Moreta G; Vinueza R; Villegas F; Mendoza-Benitez S; Guo S; Bozan N; Tos T; Incesulu A; Sennaroglu G; Blanton SH; Ozturkmen-Akay H; Yildirim-Baylan M; Tekin M Genet Med; 2016 Apr; 18(4):364-71. PubMed ID: 26226137 [TBL] [Abstract][Full Text] [Related]
33. Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing loss. Davarnia B; Babanejad M; Fattahi Z; Nikzat N; Bazazzadegan N; Pirzade A; Farajollahi R; Nishimura C; Jalalvand K; Arzhangi S; Kahrizi K; Smith RJ; Najmabadi H Int J Pediatr Otorhinolaryngol; 2012 Feb; 76(2):268-71. PubMed ID: 22172221 [TBL] [Abstract][Full Text] [Related]
34. Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing. Gao X; Zhu QY; Song YS; Wang GJ; Yuan YY; Xin F; Huang SS; Kang DY; Han MY; Guan LP; Zhang JG; Dai P J Transl Med; 2013 Nov; 11():284. PubMed ID: 24206587 [TBL] [Abstract][Full Text] [Related]
35. Report of a Novel Splicing Mutation in the Akbariazar E; Vahabi A; Abdi Rad I Clin Med Insights Case Rep; 2019; 12():1179547619871907. PubMed ID: 31579092 [TBL] [Abstract][Full Text] [Related]
36. Structure of Myo7b/USH1C complex suggests a general PDZ domain binding mode by MyTH4-FERM myosins. Li J; He Y; Weck ML; Lu Q; Tyska MJ; Zhang M Proc Natl Acad Sci U S A; 2017 May; 114(19):E3776-E3785. PubMed ID: 28439001 [TBL] [Abstract][Full Text] [Related]
37. A novel missense variant in ESRRB gene causing autosomal recessive non-syndromic hearing loss: in silico analysis of a case. Ghasemnejad T; Shekari Khaniani M; Nouri Nojadeh J; Mansoori Derakhshan S BMC Med Genomics; 2022 Feb; 15(1):18. PubMed ID: 35101039 [TBL] [Abstract][Full Text] [Related]
38. Identification and Clinical Implications of Novel MYO15A Mutations in a Non-consanguineous Korean Family by Targeted Exome Sequencing. Chang MY; Kim AR; Kim NK; Lee C; Lee KY; Jeon WS; Koo JW; Oh SH; Park WY; Kim D; Choi BY Mol Cells; 2015 Sep; 38(9):781-8. PubMed ID: 26242193 [TBL] [Abstract][Full Text] [Related]
39. MyTH4-FERM myosins have an ancient and conserved role in filopod formation. Petersen KJ; Goodson HV; Arthur AL; Luxton GW; Houdusse A; Titus MA Proc Natl Acad Sci U S A; 2016 Dec; 113(50):E8059-E8068. PubMed ID: 27911821 [TBL] [Abstract][Full Text] [Related]
40. Loss-of-function mutations in MYO15A and OTOF cause non-syndromic hearing loss in two Yemeni families. Asaad M; Mahfood M; Al Mutery A; Tlili A Hum Genomics; 2023 May; 17(1):42. PubMed ID: 37189200 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]