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.
126 related articles for article (PubMed ID: 32097363)
21. Novel compound heterozygous synonymous and missense variants in the MYO7A gene identified by next-generation sequencing in a Chinese family with nonsyndromic hearing loss. Xiang Y; Xu C; Xu Y; Zhou L; Tang S; Xu X J Clin Lab Anal; 2022 Nov; 36(11):e24708. PubMed ID: 36164746 [TBL] [Abstract][Full Text] [Related]
23. Identification of novel missense mutation related with non-syndromic sensorineural deafness, DFNA11 in korean family by NGS. Kim YR; Kim HM; Lee B; Baek JI; Lee KY; Park HJ; Kim UK Genes Genomics; 2023 Feb; 45(2):225-230. PubMed ID: 36630074 [TBL] [Abstract][Full Text] [Related]
24. A DNA variant within the MYO7A promoter regulates YY1 transcription factor binding and gene expression serving as a potential dominant DFNA11 auditory genetic modifier. Street VA; Li J; Robbins CA; Kallman JC J Biol Chem; 2011 Apr; 286(17):15278-86. PubMed ID: 21378158 [TBL] [Abstract][Full Text] [Related]
25. [Effect of inner ear hearing loss on delayed otoacoustic emissions (TEOAE) and distortion products (DPOAE)]. Hoth S Laryngorhinootologie; 1996 Dec; 75(12):709-18. PubMed ID: 9081275 [TBL] [Abstract][Full Text] [Related]
26. Spectrum of Kabahuma RI; Schubert WD; Labuschagne C; Yan D; Blanton SH; Pepper MS; Liu XZ Genes (Basel); 2021 Feb; 12(2):. PubMed ID: 33671976 [No Abstract] [Full Text] [Related]
32. Age dependence of otoacoustic emissions: the loss of amplitude is primarily caused by age-related hearing loss and not by aging alone. Hoth S; Gudmundsdottir K; Plinkert P Eur Arch Otorhinolaryngol; 2010 May; 267(5):679-90. PubMed ID: 19779930 [TBL] [Abstract][Full Text] [Related]
34. Isolated hearing loss associated with T7511C mutation in mitochondrial DNA. Yamasoba T; Tsukuda K; Suzuki M Acta Otolaryngol Suppl; 2007 Dec; (559):13-8. PubMed ID: 18340555 [TBL] [Abstract][Full Text] [Related]
35. Familial auditory neuropathy. Wang Q; Gu R; Han D; Yang W Laryngoscope; 2003 Sep; 113(9):1623-9. PubMed ID: 12972945 [TBL] [Abstract][Full Text] [Related]
36. Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss. Yamamoto N; Mutai H; Namba K; Morita N; Masuda S; Nishi Y; Nakano A; Masuda S; Fujioka M; Kaga K; Ogawa K; Matsunaga T Orphanet J Rare Dis; 2017 Sep; 12(1):157. PubMed ID: 28946916 [TBL] [Abstract][Full Text] [Related]
37. Determining the cause of hearing loss: differential diagnosis using a comparison of audiometric and otoacoustic emission responses. Mills DM Ear Hear; 2006 Oct; 27(5):508-25. PubMed ID: 16957501 [TBL] [Abstract][Full Text] [Related]
38. Identification of a novel compound heterozygous pathogenic variant in Zhang Y; Guo X; Hao L; Tian M; Ma Y; Tang Y J Int Med Res; 2023 Dec; 51(12):3000605231218924. PubMed ID: 38141656 [TBL] [Abstract][Full Text] [Related]
39. Auditory phenotype in Stickler syndrome: results of audiometric analysis in 20 patients. Acke FR; Swinnen FK; Malfait F; Dhooge IJ; De Leenheer EM Eur Arch Otorhinolaryngol; 2016 Oct; 273(10):3025-34. PubMed ID: 26786361 [TBL] [Abstract][Full Text] [Related]
40. Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11). Bolz H; Bolz SS; Schade G; Kothe C; Mohrmann G; Hess M; Gal A Hum Mutat; 2004 Sep; 24(3):274-5. PubMed ID: 15300860 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]