"P(1A8235)" . . . . "RIV/00216208:11130/06:149" . . . "5" . . . "High prevalence of the IVS 1+1 G to A/GJB2 mutation among Czech hearing impaired patients with monoallelic mutation in the coding region of GJB2"@en . . . "Vysok\u00E1 prevalence mutace IVS 1+1 G to A v GJB2 genu mezi \u010Desk\u00FDmi pacienty s poruchou sluchu a pouze jednou monoalelickou mutac\u00ED v koduj\u00EDc\u00ED oblasti GJB2 genu"@cs . "0009-9163" . "4"^^ . "69" . . "410-413" . . . . "RIV/00216208:11130/06:149!RIV07-MZ0-11130___" . "High prevalence of the IVS 1+1 G to A/GJB2 mutation among Czech hearing impaired patients with monoallelic mutation in the coding region of GJB2" . . "11130" . "[E8DF9C6CE0A0]" . . "Biallelic pathogenic GJB2 gene mutations cause pre-lingual genetic hearing loss in up to 50% of individuals with bilateral sensorineural hearing loss worldwide. Sequencing of the entire GJB2 gene-coding region in Czech patients with pre-lingual bilater" . "Seeman, Pavel" . . . . "Clinical Genetics" . "Biallelic pathogenic GJB2 gene mutations cause pre-lingual genetic hearing loss in up to 50% of individuals with bilateral sensorineural hearing loss worldwide. Sequencing of the entire GJB2 gene-coding region in Czech patients with pre-lingual bilater"@en . "477667" . . . . "High prevalence of the IVS 1+1 G to A/GJB2 mutation among Czech hearing impaired patients with monoallelic mutation in the coding region of GJB2"@en . "2"^^ . "Vysok\u00E1 prevalence mutace IVS 1+1 G to A v GJB2 genu mezi \u010Desk\u00FDmi pacienty s poruchou sluchu a pouze jednou monoalelickou mutac\u00ED v koduj\u00EDc\u00ED oblasti GJB2 genu"@cs . . "MIDWESTERN UNITED-STATES; SENSORINEURAL DEAFNESS; CONNEXIN-26 MUTATIONS; CONGENITAL DEAFNESS; EASTERN AUSTRIA; POPULATION; GENE; DEL(GJB6-D13S1830); SPECTRUM; ORIGINS"@en . "1"^^ . "DK - D\u00E1nsk\u00E9 kr\u00E1lovstv\u00ED" . "High prevalence of the IVS 1+1 G to A/GJB2 mutation among Czech hearing impaired patients with monoallelic mutation in the coding region of GJB2" . "Vysok\u00E1 prevalence mutace IVS 1+1 G to A v GJB2 genu mezi \u010Desk\u00FDmi pacienty s poruchou sluchu a pouze jednou monoalelickou mutac\u00ED v koduj\u00EDc\u00ED oblasti GJB2 genu"@cs .