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6. Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins. Rabionet R; Gasparini P; Estivill X Hum Mutat; 2000 Sep; 16(3):190-202. PubMed ID: 10980526 [TBL] [Abstract][Full Text] [Related]
7. Genetic testing for hereditary hearing loss: connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA). Prasad S; Cucci RA; Green GE; Smith RJ Hum Mutat; 2000 Dec; 16(6):502-8. PubMed ID: 11102979 [TBL] [Abstract][Full Text] [Related]
8. Aberrant gating, but a normal expression pattern, underlies the recessive phenotype of the deafness mutant Connexin26M34T. Skerrett IM; Di WL; Kasperek EM; Kelsell DP; Nicholson BJ FASEB J; 2004 May; 18(7):860-2. PubMed ID: 15033936 [TBL] [Abstract][Full Text] [Related]
9. The role of connexins in human disease. Chang EH; Van Camp G; Smith RJ Ear Hear; 2003 Aug; 24(4):314-23. PubMed ID: 12923422 [TBL] [Abstract][Full Text] [Related]
10. Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss. Kelley PM; Harris DJ; Comer BC; Askew JW; Fowler T; Smith SD; Kimberling WJ Am J Hum Genet; 1998 Apr; 62(4):792-9. PubMed ID: 9529365 [TBL] [Abstract][Full Text] [Related]
11. Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family. Kelsell DP; Wilgoss AL; Richard G; Stevens HP; Munro CS; Leigh IM Eur J Hum Genet; 2000 Jun; 8(6):469-72. PubMed ID: 10888284 [TBL] [Abstract][Full Text] [Related]
12. Pathogenetic role of the deafness-related M34T mutation of Cx26. Bicego M; Beltramello M; Melchionda S; Carella M; Piazza V; Zelante L; Bukauskas FF; Arslan E; Cama E; Pantano S; Bruzzone R; D'Andrea P; Mammano F Hum Mol Genet; 2006 Sep; 15(17):2569-87. PubMed ID: 16849369 [TBL] [Abstract][Full Text] [Related]
13. 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. Hearing loss: frequency and functional studies of the most common connexin26 alleles. D'Andrea P; Veronesi V; Bicego M; Melchionda S; Zelante L; Di Iorio E; Bruzzone R; Gasparini P Biochem Biophys Res Commun; 2002 Aug; 296(3):685-91. PubMed ID: 12176036 [TBL] [Abstract][Full Text] [Related]
16. Gap junctions and connexins in the inner ear: their roles in homeostasis and deafness. Nickel R; Forge A Curr Opin Otolaryngol Head Neck Surg; 2008 Oct; 16(5):452-7. PubMed ID: 18797288 [TBL] [Abstract][Full Text] [Related]
17. Frequencies of gap- and tight-junction mutations in Turkish families with autosomal-recessive non-syndromic hearing loss. Uyguner O; Emiroglu M; Uzumcu A; Hafiz G; Ghanbari A; Baserer N; Yuksel-Apak M; Wollnik B Clin Genet; 2003 Jul; 64(1):65-9. PubMed ID: 12791041 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Genetic analysis of the connexin-26 M34T variant. Griffith AJ J Med Genet; 2001 Jul; 38(7):E24. PubMed ID: 11432967 [No Abstract] [Full Text] [Related]
20. Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss. Cohn ES; Kelley PM Am J Med Genet; 1999 Sep; 89(3):130-6. PubMed ID: 10704187 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]