201 related articles for article (PubMed ID: 25963016)
1. High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing loss.
Mizutari K; Mutai H; Namba K; Miyanaga Y; Nakano A; Arimoto Y; Masuda S; Morimoto N; Sakamoto H; Kaga K; Matsunaga T
Orphanet J Rare Dis; 2015 May; 10():60. PubMed ID: 25963016
[TBL] [Abstract][Full Text] [Related]
2. Prevalence and clinical features of hearing loss patients with CDH23 mutations: a large cohort study.
Miyagawa M; Nishio SY; Usami S
PLoS One; 2012; 7(8):e40366. PubMed ID: 22899989
[TBL] [Abstract][Full Text] [Related]
3. Distribution and frequencies of CDH23 mutations in Japanese patients with non-syndromic hearing loss.
Wagatsuma M; Kitoh R; Suzuki H; Fukuoka H; Takumi Y; Usami S
Clin Genet; 2007 Oct; 72(4):339-44. PubMed ID: 17850630
[TBL] [Abstract][Full Text] [Related]
4. CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.
Astuto LM; Bork JM; Weston MD; Askew JW; Fields RR; Orten DJ; Ohliger SJ; Riazuddin S; Morell RJ; Khan S; Riazuddin S; Kremer H; van Hauwe P; Moller CG; Cremers CW; Ayuso C; Heckenlively JR; Rohrschneider K; Spandau U; Greenberg J; Ramesar R; Reardon W; Bitoun P; Millan J; Legge R; Friedman TB; Kimberling WJ
Am J Hum Genet; 2002 Aug; 71(2):262-75. PubMed ID: 12075507
[TBL] [Abstract][Full Text] [Related]
5. Mutations in the calcium-binding motifs of CDH23 and the 35delG mutation in GJB2 cause hearing loss in one family.
de Brouwer AP; Pennings RJ; Roeters M; Van Hauwe P; Astuto LM; Hoefsloot LH; Huygen PL; van den Helm B; Deutman AF; Bork JM; Kimberling WJ; Cremers FP; Cremers CW; Kremer H
Hum Genet; 2003 Feb; 112(2):156-63. PubMed ID: 12522556
[TBL] [Abstract][Full Text] [Related]
6. Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes.
Schultz JM; Bhatti R; Madeo AC; Turriff A; Muskett JA; Zalewski CK; King KA; Ahmed ZM; Riazuddin S; Ahmad N; Hussain Z; Qasim M; Kahn SN; Meltzer MR; Liu XZ; Munisamy M; Ghosh M; Rehm HL; Tsilou ET; Griffith AJ; Zein WM; Brewer CC; Riazuddin S; Friedman TB
J Med Genet; 2011 Nov; 48(11):767-75. PubMed ID: 21940737
[TBL] [Abstract][Full Text] [Related]
7. Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study.
Mutai H; Suzuki N; Shimizu A; Torii C; Namba K; Morimoto N; Kudoh J; Kaga K; Kosaki K; Matsunaga T
Orphanet J Rare Dis; 2013 Oct; 8():172. PubMed ID: 24164807
[TBL] [Abstract][Full Text] [Related]
8. Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.
Green GE; Scott DA; McDonald JM; Woodworth GG; Sheffield VC; Smith RJ
JAMA; 1999 Jun; 281(23):2211-6. PubMed ID: 10376574
[TBL] [Abstract][Full Text] [Related]
9. Patients with CDH23 mutations and the 1555A>G mitochondrial mutation are good candidates for electric acoustic stimulation (EAS).
Usami S; Miyagawa M; Nishio SY; Moteki H; Takumi Y; Suzuki M; Kitano Y; Iwasaki S
Acta Otolaryngol; 2012 Apr; 132(4):377-84. PubMed ID: 22443853
[TBL] [Abstract][Full Text] [Related]
10. GJB2 (Cx26) gene mutations in Chinese patients with congenital sensorineural deafness and a report of one novel mutation.
Xiao ZA; Xie DH
Chin Med J (Engl); 2004 Dec; 117(12):1797-801. PubMed ID: 15603707
[TBL] [Abstract][Full Text] [Related]
11. An ENU-induced mutation of Cdh23 causes congenital hearing loss, but no vestibular dysfunction, in mice.
Manji SS; Miller KA; Williams LH; Andreasen L; Siboe M; Rose E; Bahlo M; Kuiper M; Dahl HH
Am J Pathol; 2011 Aug; 179(2):903-14. PubMed ID: 21689626
[TBL] [Abstract][Full Text] [Related]
12. [Analysis of positive rate of common genetic mutations in 1448 cases with different hearing phenotype].
Wang G; Yuan Y; Li R; Han M; Huang S; Kang D; Zhang X; Dong M; Dai P; Han D
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2011 May; 25(10):445-8. PubMed ID: 21809555
[TBL] [Abstract][Full Text] [Related]
13. Identification and in vitro expression of novel CDH23 mutations of patients with Usher syndrome type 1D.
von Brederlow B; Bolz H; Janecke A; La O Cabrera A; Rudolph G; Lorenz B; Schwinger E; Gal A
Hum Mutat; 2002 Mar; 19(3):268-73. PubMed ID: 11857743
[TBL] [Abstract][Full Text] [Related]
14. Variants in CDH23 cause a broad spectrum of hearing loss: from non-syndromic to syndromic hearing loss as well as from congenital to age-related hearing loss.
Usami SI; Isaka Y; Miyagawa M; Nishio SY
Hum Genet; 2022 Apr; 141(3-4):903-914. PubMed ID: 35020051
[TBL] [Abstract][Full Text] [Related]
15. Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing.
Woo HM; Park HJ; Park MH; Kim BY; Shin JW; Yoo WG; Koo SK
BMC Med Genet; 2014 Apr; 15():46. PubMed ID: 24767429
[TBL] [Abstract][Full Text] [Related]
16. A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families.
Riahi Z; Chahed H; Jaafoura H; Zainine R; Messaoud O; Naili M; Nagara M; Hammami H; Laroussi N; Bouyacoub Y; Kefi R; Bonnet C; Besbes G; Abdelhak S
Int J Pediatr Otorhinolaryngol; 2013 Sep; 77(9):1485-8. PubMed ID: 23856379
[TBL] [Abstract][Full Text] [Related]
17. Strong founder effect of p.P240L in CDH23 in Koreans and its significant contribution to severe-to-profound nonsyndromic hearing loss in a Korean pediatric population.
Kim SY; Kim AR; Kim NK; Kim MY; Jeon EH; Kim BJ; Han YE; Chang MY; Park WY; Choi BY
J Transl Med; 2015 Aug; 13():263. PubMed ID: 26264712
[TBL] [Abstract][Full Text] [Related]
18. Genetic Predisposition to Sporadic Congenital Hearing Loss in a Pediatric Population.
Jung J; Lee JS; Cho KJ; Yu S; Yoon JH; Yung Gee H; Choi JY
Sci Rep; 2017 Apr; 7():45973. PubMed ID: 28383030
[TBL] [Abstract][Full Text] [Related]
19. Discovery of CDH23 as a Significant Contributor to Progressive Postlingual Sensorineural Hearing Loss in Koreans.
Kim BJ; Kim AR; Lee C; Kim SY; Kim NK; Chang MY; Rhee J; Park MH; Koo SK; Kim MY; Han JH; Oh SH; Park WY; Choi BY
PLoS One; 2016; 11(10):e0165680. PubMed ID: 27792758
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
