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.
159 related articles for article (PubMed ID: 15996214)
1. Functional analysis of R75Q mutation in the gene coding for Connexin 26 identified in a family with nonsyndromic hearing loss. Piazza V; Beltramello M; Menniti M; Colao E; Malatesta P; Argento R; Chiarella G; Gallo LV; Catalano M; Perrotti N; Mammano F; Cassandro E Clin Genet; 2005 Aug; 68(2):161-6. PubMed ID: 15996214 [TBL] [Abstract][Full Text] [Related]
2. R75Q de novo dominant mutation of GJB2 in a Chinese family with hearing loss and palmoplantar keratoderma. Jiang SJ; Di ZH; Huang D; Zhang JB; Zhang YY; Li SQ; He R Int J Pediatr Otorhinolaryngol; 2014 Sep; 78(9):1461-6. PubMed ID: 24975403 [TBL] [Abstract][Full Text] [Related]
3. Intra-familial phenotypic variability in a Moroccan family with hearing loss and palmoplantar keratoderma (PPK). Bousfiha A; Bakhchane A; Elrharchi S; Dehbi H; Kabine M; Nadifi S; Charoute H; Barakat A Curr Res Transl Med; 2016; 64(2):61-4. PubMed ID: 27316387 [TBL] [Abstract][Full Text] [Related]
4. The novel R75Q mutation in the GJB2 gene causes autosomal dominant hearing loss and palmoplantar keratoderma in a Turkish family. Uyguner O; Tukel T; Baykal C; Eris H; Emiroglu M; Hafiz G; Ghanbari A; Baserer N; Yuksel-Apak M; Wollnik B Clin Genet; 2002 Oct; 62(4):306-9. PubMed ID: 12372058 [TBL] [Abstract][Full Text] [Related]
5. New evidence for the correlation of the p.G130V mutation in the GJB2 gene and syndromic hearing loss with palmoplantar keratoderma. Iossa S; Chinetti V; Auletta G; Laria C; De Luca M; Rienzo M; Giannini P; Delfino M; Ciccodicola A; Marciano E; Franzé A Am J Med Genet A; 2009 Feb; 149A(4):685-8. PubMed ID: 18688874 [TBL] [Abstract][Full Text] [Related]
6. trans-dominant inhibition of connexin-43 by mutant connexin-26: implications for dominant connexin disorders affecting epidermal differentiation. Rouan F; White TW; Brown N; Taylor AM; Lucke TW; Paul DL; Munro CS; Uitto J; Hodgins MB; Richard G J Cell Sci; 2001 Jun; 114(Pt 11):2105-13. PubMed ID: 11493646 [TBL] [Abstract][Full Text] [Related]
7. A connexin 26 mutation causes a syndrome of sensorineural hearing loss and palmoplantar hyperkeratosis (MIM 148350). Heathcote K; Syrris P; Carter ND; Patton MA J Med Genet; 2000 Jan; 37(1):50-1. PubMed ID: 10633135 [TBL] [Abstract][Full Text] [Related]
8. Autosomal dominant prelingual hearing loss with palmoplantar keratoderma syndrome: Variability in clinical expression from mutations of R75W and R75Q in the GJB2 gene. Birkenhäger R; Lüblinghoff N; Prera E; Schild C; Aschendorff A; Arndt S Am J Med Genet A; 2010 Jul; 152A(7):1798-802. PubMed ID: 20583176 [TBL] [Abstract][Full Text] [Related]
9. Autosomal dominant hearing loss resulting from p.R75Q mutation in the GJB2 gene: nonsyndromic presentation in a South Indian family. Pavithra A; Selvakumari M; Nityaa V; Sharanya N; Ramakrishnan R; Narasimhan M; Srisailapathy CR Ann Hum Genet; 2015 Jan; 79(1):76-82. PubMed ID: 25393658 [TBL] [Abstract][Full Text] [Related]
10. Expanding the phenotypic spectrum of Cx26 disorders: Bart-Pumphrey syndrome is caused by a novel missense mutation in GJB2. Richard G; Brown N; Ishida-Yamamoto A; Krol A J Invest Dermatol; 2004 Nov; 123(5):856-63. PubMed ID: 15482471 [TBL] [Abstract][Full Text] [Related]
11. A mild phenotype of sensorineural hearing loss and palmoplantar keratoderma caused by a novel GJB2 dominant mutation. Stanghellini I; Genovese E; Palma S; Falcinelli C; Presutti L; Percesepe A Acta Otorhinolaryngol Ital; 2017 Aug; 37(4):308-311. PubMed ID: 28872160 [TBL] [Abstract][Full Text] [Related]
12. A novel missense mutation in the second extracellular domain of GJB2, p.Ser183Phe, causes a syndrome of focal palmoplantar keratoderma with deafness. de Zwart-Storm EA; van Geel M; van Neer PA; Steijlen PM; Martin PE; van Steensel MA Am J Pathol; 2008 Oct; 173(4):1113-9. PubMed ID: 18787097 [TBL] [Abstract][Full Text] [Related]
13. A novel missense mutation in GJB2 disturbs gap junction protein transport and causes focal palmoplantar keratoderma with deafness. de Zwart-Storm EA; Hamm H; Stoevesandt J; Steijlen PM; Martin PE; van Geel M; van Steensel MA J Med Genet; 2008 Mar; 45(3):161-6. PubMed ID: 17993581 [TBL] [Abstract][Full Text] [Related]
14. Hereditary palmoplantar keratoderma and deafness resulting from genetic mutation of Connexin 26. Lee JY; In SI; Kim HJ; Jeong SY; Choung YH; Kim YC J Korean Med Sci; 2010 Oct; 25(10):1539-42. PubMed ID: 20890442 [TBL] [Abstract][Full Text] [Related]
15. Connexin 26 mutation in keratitis-ichthyosis-deafness (KID) syndrome in mother and daughter with combined conductive and sensorineural hearing loss. Kelly B; Lozano A; Altenberg G; Makishima T Int J Dermatol; 2008 May; 47(5):443-7. PubMed ID: 18412859 [TBL] [Abstract][Full Text] [Related]
16. G130V de novo mutation in an Iranian pedigree with nonsyndromic hearing loss without palmoplantar keratoderma. Babanejad M; Zarandy MM; Nikzat N; Bazazzadegan N; Arzhangi S; Mohseni M; Kahrizi K; Najmabadi H Int J Pediatr Otorhinolaryngol; 2019 Nov; 126():109607. PubMed ID: 31419744 [TBL] [Abstract][Full Text] [Related]
17. A de novo GJB2 (connexin 26) mutation, R75W, in a Chinese pedigree with hearing loss and palmoplantar keratoderma. Yuan Y; Huang D; Yu F; Zhu X; Kang D; Yuan H; Han D; Dai P Am J Med Genet A; 2009 Feb; 149A(4):689-92. PubMed ID: 18924167 [No Abstract] [Full Text] [Related]
18. De novo mutation of the connexin 26 gene associated with dominant non-syndromic sensorineural hearing loss. Janecke AR; Nekahm D; Löffler J; Hirst-Stadlmann A; Müller T; Utermann G Hum Genet; 2001 Mar; 108(3):269-70. PubMed ID: 11354642 [TBL] [Abstract][Full Text] [Related]
19. Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma. Richard G; White TW; Smith LE; Bailey RA; Compton JG; Paul DL; Bale SJ Hum Genet; 1998 Oct; 103(4):393-9. PubMed ID: 9856479 [TBL] [Abstract][Full Text] [Related]
20. Missense mutations in GJB2 encoding connexin-26 cause the ectodermal dysplasia keratitis-ichthyosis-deafness syndrome. Richard G; Rouan F; Willoughby CE; Brown N; Chung P; Ryynänen M; Jabs EW; Bale SJ; DiGiovanna JJ; Uitto J; Russell L Am J Hum Genet; 2002 May; 70(5):1341-8. PubMed ID: 11912510 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]