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.
242 related articles for article (PubMed ID: 10369879)
1. Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families. Coucke PJ; Van Hauwe P; Kelley PM; Kunst H; Schatteman I; Van Velzen D; Meyers J; Ensink RJ; Verstreken M; Declau F; Marres H; Kastury K; Bhasin S; McGuirt WT; Smith RJ; Cremers CW; Van de Heyning P; Willems PJ; Smith SD; Van Camp G Hum Mol Genet; 1999 Jul; 8(7):1321-8. PubMed ID: 10369879 [TBL] [Abstract][Full Text] [Related]
2. Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region. Van Hauwe P; Coucke PJ; Ensink RJ; Huygen P; Cremers CW; Van Camp G Am J Med Genet; 2000 Jul; 93(3):184-7. PubMed ID: 10925378 [TBL] [Abstract][Full Text] [Related]
3. Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss. Talebizadeh Z; Kelley PM; Askew JW; Beisel KW; Smith SD Hum Mutat; 1999; 14(6):493-501. PubMed ID: 10571947 [TBL] [Abstract][Full Text] [Related]
4. Further evidence for a third deafness gene within the DFNA2 locus. Goldstein JA; Lalwani AK Am J Med Genet; 2002 Apr; 108(4):304-9. PubMed ID: 11920835 [TBL] [Abstract][Full Text] [Related]
5. The DFNA2 locus for hearing impairment: two genes regulating K+ ion recycling in the inner ear. Van Hauwe P; Coucke P; Van Camp G Br J Audiol; 1999 Oct; 33(5):285-9. PubMed ID: 10890142 [TBL] [Abstract][Full Text] [Related]
6. A mutational hot spot in the KCNQ4 gene responsible for autosomal dominant hearing impairment. Van Camp G; Coucke PJ; Akita J; Fransen E; Abe S; De Leenheer EM; Huygen PL; Cremers CW; Usami S Hum Mutat; 2002 Jul; 20(1):15-9. PubMed ID: 12112653 [TBL] [Abstract][Full Text] [Related]
7. A novel pore-region mutation, c.887G > A (p.G296D) in KCNQ4, causing hearing loss in a Chinese family with autosomal dominant non-syndromic deafness 2. Huang B; Liu Y; Gao X; Xu J; Dai P; Zhu Q; Yuan Y BMC Med Genet; 2017 Mar; 18(1):36. PubMed ID: 28340560 [TBL] [Abstract][Full Text] [Related]
8. KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness. Kubisch C; Schroeder BC; Friedrich T; Lütjohann B; El-Amraoui A; Marlin S; Petit C; Jentsch TJ Cell; 1999 Feb; 96(3):437-46. PubMed ID: 10025409 [TBL] [Abstract][Full Text] [Related]
9. Targeted high-throughput sequencing identifies pathogenic mutations in KCNQ4 in two large Chinese families with autosomal dominant hearing loss. Wang H; Zhao Y; Yi Y; Gao Y; Liu Q; Wang D; Li Q; Lan L; Li N; Guan J; Yin Z; Han B; Zhao F; Zong L; Xiong W; Yu L; Song L; Yi X; Yang L; Petit C; Wang Q PLoS One; 2014; 9(8):e103133. PubMed ID: 25116015 [TBL] [Abstract][Full Text] [Related]
10. Genetics of hearing loss: focus on DFNA2. Dominguez LM; Dodson KM Appl Clin Genet; 2012; 5():97-104. PubMed ID: 23776385 [TBL] [Abstract][Full Text] [Related]
11. A recurrent mutation in KCNQ4 in Korean families with nonsyndromic hearing loss and rescue of the channel activity by KCNQ activators. Shin DH; Jung J; Koh YI; Rim JH; Lee JS; Choi HJ; Joo SY; Yu S; Cha DH; Lee SY; Lee JH; Lee MG; Choi JY; Gee HY Hum Mutat; 2019 Mar; 40(3):335-346. PubMed ID: 30556268 [TBL] [Abstract][Full Text] [Related]
12. Identification of novel mutations in the KCNQ4 gene of patients with nonsyndromic deafness from Taiwan. Su CC; Yang JJ; Shieh JC; Su MC; Li SY Audiol Neurootol; 2007; 12(1):20-6. PubMed ID: 17033161 [TBL] [Abstract][Full Text] [Related]
13. Whole-exome sequencing identifies two novel mutations in KCNQ4 in individuals with nonsyndromic hearing loss. Jung J; Choi HB; Koh YI; Rim JH; Choi HJ; Kim SH; Lee JH; An J; Kim A; Lee JS; Joo SY; Yu S; Choi JY; Kang TM; Gee HY Sci Rep; 2018 Nov; 8(1):16659. PubMed ID: 30413759 [TBL] [Abstract][Full Text] [Related]
14. A novel Li Q; Liang P; Wang S; Li W; Wang J; Yang Y; An X; Chen J; Zha D Mol Med Rep; 2021 Jun; 23(6):. PubMed ID: 33846771 [TBL] [Abstract][Full Text] [Related]
15. Audioprofile-directed screening identifies novel mutations in KCNQ4 causing hearing loss at the DFNA2 locus. Hildebrand MS; Tack D; McMordie SJ; DeLuca A; Hur IA; Nishimura C; Huygen P; Casavant TL; Smith RJ Genet Med; 2008 Nov; 10(11):797-804. PubMed ID: 18941426 [TBL] [Abstract][Full Text] [Related]
16. Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss: KCNQ4 is a gene responsible in Japanese. Akita J; Abe S; Shinkawa H; Kimberling WJ; Usami S J Hum Genet; 2001; 46(7):355-61. PubMed ID: 11450843 [TBL] [Abstract][Full Text] [Related]
17. [KCNQ4 gene mutations affected a pedigree with autosomal dominant hereditary hearing loss]. Wang Q; Cao J; Li N; Yang Y; Wang Q; Yu L; Han D; Yang W Zhonghua Er Bi Yan Hou Ke Za Zhi; 2002 Oct; 37(5):343-7. PubMed ID: 12772453 [TBL] [Abstract][Full Text] [Related]
18. Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCH. Bom SJ; De Leenheer EM; Lemaire FX; Kemperman MH; Verhagen WI; Marres HA; Kunst HP; Ensink RJ; Bosman AJ; Van Camp G; Cremers FP; Huygen PL; Cremers CW Arch Otolaryngol Head Neck Surg; 2001 Sep; 127(9):1045-8. PubMed ID: 11556850 [TBL] [Abstract][Full Text] [Related]
19. Audiologic evidence for further genetic heterogeneity at DFNA2. Stern RE; Lalwani AK Acta Otolaryngol; 2002 Oct; 122(7):730-5. PubMed ID: 12484650 [TBL] [Abstract][Full Text] [Related]