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4. Audiologic Phenotype and Progression in Pediatric STRC-Related Autosomal Recessive Hearing Loss. Simi A; Perry J; Schindler E; Oza A; Luo M; Hartman T; Krantz ID; Germiller JA; Kawai K; Kenna M Laryngoscope; 2021 Dec; 131(12):E2897-E2903. PubMed ID: 34111299 [TBL] [Abstract][Full Text] [Related]
5. Early audiological phenotype in patients with mutations in the USH2A gene. Markova TG; Lalayants MR; Alekseeva NN; Ryzhkova OP; Shatokhina OL; Galeeva NM; Bliznetz EA; Weener ME; Belov OA; Chibisova SS; Polyakov AV; Tavartkiladze GA Int J Pediatr Otorhinolaryngol; 2022 Jun; 157():111140. PubMed ID: 35452909 [TBL] [Abstract][Full Text] [Related]
6. Clinical features of hearing loss caused by STRC gene deletions/mutations in Russian population. Markova TG; Alekseeva NN; Mironovich OL; Galeeva NM; Lalayants MR; Bliznetz EA; Chibisova SS; Polyakov AV; Tavartkiladze GA Int J Pediatr Otorhinolaryngol; 2020 Nov; 138():110247. PubMed ID: 32705992 [TBL] [Abstract][Full Text] [Related]
7. STRC Gene Mutations, Mainly Large Deletions, are a Very Important Cause of Early-Onset Hereditary Hearing Loss in the Czech Population. Marková SP; Brožková DŠ; Laššuthová P; Mészárosová A; Krůtová M; Neupauerová J; Rašková D; Trková M; Staněk D; Seeman P Genet Test Mol Biomarkers; 2018 Feb; 22(2):127-134. PubMed ID: 29425068 [TBL] [Abstract][Full Text] [Related]
8. Spectrum and frequencies of non GJB2 gene mutations in Czech patients with early non-syndromic hearing loss detected by gene panel NGS and whole-exome sequencing. Safka Brozkova D; Poisson Marková S; Mészárosová AU; Jenčík J; Čejnová V; Čada Z; Laštůvková J; Rašková D; Seeman P Clin Genet; 2020 Dec; 98(6):548-554. PubMed ID: 32860223 [TBL] [Abstract][Full Text] [Related]
9. Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment. Francey LJ; Conlin LK; Kadesch HE; Clark D; Berrodin D; Sun Y; Glessner J; Hakonarson H; Jalas C; Landau C; Spinner NB; Kenna M; Sagi M; Rehm HL; Krantz ID Am J Med Genet A; 2012 Feb; 158A(2):298-308. PubMed ID: 22147502 [TBL] [Abstract][Full Text] [Related]
10. [Hearing loss due to mutations or lack of the gene coding protein stereocillin]. Markova TG; Alekseeva NN; Mironovich OL; Bliznets EA; Lalayants MR; Polyakov AV; Tavartkiladze GA Vestn Otorinolaringol; 2020; 85(2):14-20. PubMed ID: 32476383 [TBL] [Abstract][Full Text] [Related]
11. Prevalence and Characteristics of STRC Gene Mutations (DFNB16): A Systematic Review and Meta-Analysis. Han S; Zhang D; Guo Y; Fu Z; Guan G Front Genet; 2021; 12():707845. PubMed ID: 34621290 [No Abstract] [Full Text] [Related]
12. Frequency and clinical features of hearing loss caused by STRC deletions. Yokota Y; Moteki H; Nishio SY; Yamaguchi T; Wakui K; Kobayashi Y; Ohyama K; Miyazaki H; Matsuoka R; Abe S; Kumakawa K; Takahashi M; Sakaguchi H; Uehara N; Ishino T; Kosho T; Fukushima Y; Usami SI Sci Rep; 2019 Mar; 9(1):4408. PubMed ID: 30867468 [TBL] [Abstract][Full Text] [Related]
13. Spectrum of Genes for Non- Shatokhina O; Galeeva N; Stepanova A; Markova T; Lalayants M; Alekseeva N; Tavarkiladze G; Markova T; Bessonova L; Petukhova M; Guseva D; Anisimova I; Polyakov A; Ryzhkova O; Bliznetz E Int J Mol Sci; 2022 Dec; 23(24):. PubMed ID: 36555390 [TBL] [Abstract][Full Text] [Related]
14. Identification of a nonsense mutation in the STRC gene in a Korean family with moderate hearing loss. Sagong B; Baek JI; Bok J; Lee KY; Kim UK Int J Pediatr Otorhinolaryngol; 2016 Jan; 80():78-81. PubMed ID: 26746617 [TBL] [Abstract][Full Text] [Related]
15. [The audiological phenotype and the prevalence of GJB2-related sensorineural loss of hearing in the infants suffering acoustic disturbances]. Lalaiants MR; Markova TG; Bakhshinian VV; Bliznets EA; Poliakov AV; Tavartikiladze GA Vestn Otorinolaringol; 2014; (2):37-43. PubMed ID: 24781170 [TBL] [Abstract][Full Text] [Related]
16. [Genetic characteristic analysis of slight-to-moderate sensorineural hearing loss in children]. Zhou R; Guan J; Wang Q Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2024 Jan; 38(1):18-22. PubMed ID: 38297844 [No Abstract] [Full Text] [Related]
17. GJB2 mutations and genotype-phenotype correlation in 335 patients from germany with nonsyndromic sensorineural hearing loss: evidence for additional recessive mutations not detected by current methods. Bartsch O; Vatter A; Zechner U; Kohlschmidt N; Wetzig C; Baumgart A; Nospes S; Haaf T; Keilmann A Audiol Neurootol; 2010; 15(6):375-82. PubMed ID: 20234132 [TBL] [Abstract][Full Text] [Related]
18. STRC Deletion is a Frequent Cause of Slight to Moderate Congenital Hearing Impairment in the Czech Republic. Plevova P; Paprskarova M; Tvrda P; Turska P; Slavkovsky R; Mrazkova E Otol Neurotol; 2017 Dec; 38(10):e393-e400. PubMed ID: 28984810 [TBL] [Abstract][Full Text] [Related]
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