<p>Allele frequencies of reference sequence nucleotides are provided for each DNA sequence variant. n = the number of chromosomes studied. <i>P</i> values are calculated by comparing patients to the combined control group. Novel variants are shown in bold type.</p
<p>N, number;</p><p>*<i>p</i> value <0.05 is statistically significant.</p><p>Comparison of ACE geno...
The expected allele percentage was measured and specified by the manufacturer using digital PCR or n...
<p>The bold black letters denote the novel mutations, “N” indicates the normal SLC25A13 allele, whil...
<p>Heterozygosity is provided for each DNA sequence variation. n = the number of individuals studied...
<p>Additional sequence variations observed in the patient and control samples heterozygous for the <...
<p>Haplotype blocks as determined by HaploView 4.0 are shown as shaded bars and compared for patient...
1<p>Wet lab confirmation of variant by sequenced PCR products using target specific primers.</p>2<p>...
<p>Molecular epidemiological information of ten <i>SLC26A4</i> variants in 2352 unrelated NSHL patie...
<p>DNA from each donor was extracted from separate buccal swabs (left or right sides) and blood and ...
<p>Fisher's exact test <i>p</i> values calculated for 231 variants in 57 patients and 1100 participa...
<p>The forearms of two donors were marked with a template indicating five 25 x 25 mm squares (Upper ...
<p>The risk alleles considered are the variant alleles of rs7574865, rs3099844 and rs3024505 SNPs.</...
<p>Key: Heterozygous, Het; Homozygous, Homo; Familial, FM; Sporadic, SP; Not available, n.a.</p><p>*...
<p>(A) Each column represents analyses of all DNA sequence variants in 3′ UTRs (3′ UTR) or variants ...
<p>The genotypic and allelic frequencies of rs2275913, rs763780 and rs4819554 between cases and cont...
<p>N, number;</p><p>*<i>p</i> value <0.05 is statistically significant.</p><p>Comparison of ACE geno...
The expected allele percentage was measured and specified by the manufacturer using digital PCR or n...
<p>The bold black letters denote the novel mutations, “N” indicates the normal SLC25A13 allele, whil...
<p>Heterozygosity is provided for each DNA sequence variation. n = the number of individuals studied...
<p>Additional sequence variations observed in the patient and control samples heterozygous for the <...
<p>Haplotype blocks as determined by HaploView 4.0 are shown as shaded bars and compared for patient...
1<p>Wet lab confirmation of variant by sequenced PCR products using target specific primers.</p>2<p>...
<p>Molecular epidemiological information of ten <i>SLC26A4</i> variants in 2352 unrelated NSHL patie...
<p>DNA from each donor was extracted from separate buccal swabs (left or right sides) and blood and ...
<p>Fisher's exact test <i>p</i> values calculated for 231 variants in 57 patients and 1100 participa...
<p>The forearms of two donors were marked with a template indicating five 25 x 25 mm squares (Upper ...
<p>The risk alleles considered are the variant alleles of rs7574865, rs3099844 and rs3024505 SNPs.</...
<p>Key: Heterozygous, Het; Homozygous, Homo; Familial, FM; Sporadic, SP; Not available, n.a.</p><p>*...
<p>(A) Each column represents analyses of all DNA sequence variants in 3′ UTRs (3′ UTR) or variants ...
<p>The genotypic and allelic frequencies of rs2275913, rs763780 and rs4819554 between cases and cont...
<p>N, number;</p><p>*<i>p</i> value <0.05 is statistically significant.</p><p>Comparison of ACE geno...
The expected allele percentage was measured and specified by the manufacturer using digital PCR or n...
<p>The bold black letters denote the novel mutations, “N” indicates the normal SLC25A13 allele, whil...
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