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A. Solovyev V.
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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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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
якуты
founder effect
Якутия
ген FYCO1
эффект основателя
CLIC5 gene
CTRCT18
Chukchi’s population
DFNB103
Evens
FYCO1
FYCO1 gene
GJB2 gene
Sakha Republic
UCP1 gene
UCP2 gene
UCP3 gene
Yakutia
Yakuts population
Yukaghirs
c.-23+1G>A mutation
congenital autosomal recessive cataract
congenital cataract
frequency of heterozygous carrier
hearing loss
juvenile autosomal recessive deafness
population isolate
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