600 related articles for article (PubMed ID: 23151025)
1. Identification of SLC26A4 c.919-2A>G compound heterozygosity in hearing-impaired patients to improve genetic counseling.
Li Q; Zhu QW; Yuan YY; Huang SS; Han DY; Huang DL; Dai P
J Transl Med; 2012 Nov; 10():225. PubMed ID: 23151025
[TBL] [Abstract][Full Text] [Related]
2. [Sequencing analysis of whole SLC26A4 gene in severe to profound sensorineural hearing loss patients with IVS7-2A to G mutation of the gene].
Li Q; Huang DL; Zhu QW; Yuan YY; Fang RP; Dai P
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Dec; 27(6):610-5. PubMed ID: 21154317
[TBL] [Abstract][Full Text] [Related]
3. Novel compound heterozygous mutations in SLC26A4 gene in a Chinese family with enlarged vestibular aqueduct.
Zhao X; Cheng X; Huang L; Wang X; Wen C; Wang X
Biosci Trends; 2018; 12(5):502-506. PubMed ID: 30473558
[TBL] [Abstract][Full Text] [Related]
4. Mono-allelic mutations of SLC26A4 is over-presented in deaf patients with non-syndromic enlarged vestibular aqueduct.
Pang X; Chai Y; Chen P; He L; Wang X; Wu H; Yang T
Int J Pediatr Otorhinolaryngol; 2015 Aug; 79(8):1351-3. PubMed ID: 26100058
[TBL] [Abstract][Full Text] [Related]
5. [Sequencing analysis of whole SLC26A4 gene related to IVS7-2A > G mutation in 1552 moderate to profound sensorineural hearing loss patients in China].
Yuan YY; Dai P; Zhu QW; Kang DY; Huang DL
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2009 Jun; 44(6):449-54. PubMed ID: 19954013
[TBL] [Abstract][Full Text] [Related]
6. Low frequency of SLC26A4 c.919-2A > G variant among patients with nonsyndromic hearing loss in Yunnan of Southwest China.
Li YQ; Ma H; Wang QY; Liu DS; Wang W; Li SX; Zuo RX; Shen T; Zhu BS; Sa YL
BMC Med Genomics; 2024 Feb; 17(1):55. PubMed ID: 38378613
[TBL] [Abstract][Full Text] [Related]
7. Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss.
Dai P; Stewart AK; Chebib F; Hsu A; Rozenfeld J; Huang D; Kang D; Lip V; Fang H; Shao H; Liu X; Yu F; Yuan H; Kenna M; Miller DT; Shen Y; Yang W; Zelikovic I; Platt OS; Han D; Alper SL; Wu BL
Physiol Genomics; 2009 Aug; 38(3):281-90. PubMed ID: 19509082
[TBL] [Abstract][Full Text] [Related]
8. [An investigation of SLC26A4 gene mutation in nonsydromic hearing impairment in Hunan province of China].
Jiang L; Feng Y; Chen H; He C; Mei L
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2010 Jul; 24(13):587-91. PubMed ID: 20842945
[TBL] [Abstract][Full Text] [Related]
9. Molecular analysis of SLC26A4 gene in patients with nonsyndromic hearing loss and EVA: identification of two novel mutations in Brazilian patients.
de Moraes VC; dos Santos NZ; Ramos PZ; Svidnicki MC; Castilho AM; Sartorato EL
Int J Pediatr Otorhinolaryngol; 2013 Mar; 77(3):410-3. PubMed ID: 23273637
[TBL] [Abstract][Full Text] [Related]
10. Novel heterozygous mutation c.662_663insG compound with IVS7-2A>G mutation in SLC26A4 gene in a Chinese family with Pendred syndrome.
Chen K; Zhou W; Zong L; Liu M; Du J; Jiang H
Int J Pediatr Otorhinolaryngol; 2012 Nov; 76(11):1633-6. PubMed ID: 22906308
[TBL] [Abstract][Full Text] [Related]
11. Genotyping and audiological characteristics of infants with a single-allele SLC26A4 mutation.
Zhao X; Huang L; Wang X; Wang X; Zhao L; Cheng X; Ruan Y
Int J Pediatr Otorhinolaryngol; 2019 Jan; 116():153-158. PubMed ID: 30554688
[TBL] [Abstract][Full Text] [Related]
12. Compound heterozygous mutations of SLC26A4 in 4 Chinese families with enlarged vestibular aqueduct.
Yao G; Li S; Chen D; Wang H; Zhang J; Feng Z; Guo L; Yang Z; Yang S; Sun C; Zhang X; Ma D
Int J Pediatr Otorhinolaryngol; 2013 Apr; 77(4):544-9. PubMed ID: 23385134
[TBL] [Abstract][Full Text] [Related]
13. Molecular epidemiology and functional assessment of novel allelic variants of SLC26A4 in non-syndromic hearing loss patients with enlarged vestibular aqueduct in China.
Yuan Y; Guo W; Tang J; Zhang G; Wang G; Han M; Zhang X; Yang S; He DZ; Dai P
PLoS One; 2012; 7(11):e49984. PubMed ID: 23185506
[TBL] [Abstract][Full Text] [Related]
14. SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss.
Dai P; Li Q; Huang D; Yuan Y; Kang D; Miller DT; Shao H; Zhu Q; He J; Yu F; Liu X; Han B; Yuan H; Platt OS; Han D; Wu BL
Genet Med; 2008 Aug; 10(8):586-92. PubMed ID: 18641518
[TBL] [Abstract][Full Text] [Related]
15. Mutation analysis of the SLC26A4 gene in three Chinese families.
Wen C; Wang S; Zhao X; Wang X; Wang X; Cheng X; Huang L
Biosci Trends; 2019 Nov; 13(5):441-447. PubMed ID: 31656273
[TBL] [Abstract][Full Text] [Related]
16. Molecular etiology of hearing impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysis.
Dai P; Yuan Y; Huang D; Zhu X; Yu F; Kang D; Yuan H; Wu B; Han D; Wong LJ
J Transl Med; 2008 Nov; 6():74. PubMed ID: 19040761
[TBL] [Abstract][Full Text] [Related]
17. Probing the Effect of Two Heterozygous Mutations in Codon 723 of SLC26A4 on Deafness Phenotype Based on Molecular Dynamics Simulations.
Yao J; Qian X; Bao J; Wei Q; Lu Y; Zheng H; Cao X; Xing G
Sci Rep; 2015 Jun; 5():10831. PubMed ID: 26035154
[TBL] [Abstract][Full Text] [Related]
18. Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing-impaired subjects.
Nonose RW; Lezirovitz K; de Mello Auricchio MTB; Batissoco AC; Yamamoto GL; Mingroni-Netto RC
BMC Med Genet; 2018 May; 19(1):73. PubMed ID: 29739340
[TBL] [Abstract][Full Text] [Related]
19. [Mutational screening of the SLC26A4 gene in patients with nonsyndromic hearing loss by denaturing high-performance liquid chromatography].
Zhao J; Wu LQ; Feng Y; Pan Q; Zhao K; Li HY; Liang DS
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb; 26(1):21-5. PubMed ID: 19199245
[TBL] [Abstract][Full Text] [Related]
20. Correlation between genotype and phenotype in patients with bi-allelic SLC26A4 mutations.
Lee HJ; Jung J; Shin JW; Song MH; Kim SH; Lee JH; Lee KA; Shin S; Kim UK; Bok J; Lee KY; Choi JY; Park HJ
Clin Genet; 2014 Sep; 86(3):270-5. PubMed ID: 24007330
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]