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Bioethical aspects of DNA testing of inherited hearing disorders in Yakutia
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Reconstruction of the founder haplotype with mutation c.644G>A p. (Trp215*) in t...
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Analysis of polymorphism of SNP markers of genes involved in nonshivering thermo...
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Mutation analysis of the SLC26A4 gene in patients in Yakutia with inner ear abno...
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Novel transition c.1621C>T (p.Gln541*) in the FYCO1 gene is a major cause of con...
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Autosomal recessive cataract (CTRCT18) in Yakutia: results of molecular genetic...
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Related Subjects
Eastern Siberia
Yakuts
Восточная Сибирь
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founder effect
ген FYCO1
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congenital autosomal recessive cataract
congenital cataract
congenital deafness
frequency of heterozygous carrier
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