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Ф. Терютин М.
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Ф. Терютин М.
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Reconstruction of the founder haplotype with mutation c.644G>A p. (Trp215*) in t...
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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
якуты
founder effect
Якутия
ген FYCO1
эффект основателя
CLIC5 gene
CTRCT18
DFNB103
DFNB4
Evens
FYCO1
FYCO1 gene
SLC26A4 gene
Sakha Republic
Yakutia
Yukaghirs
congenital autosomal recessive cataract
congenital cataract
congenital deafness
inner ear abnormalities
juvenile autosomal recessive deafness
population isolate
variant c644G>
аномалии внутреннего уха
врожденная аутосомно-рецессивная катаракта
врожденная глухота
врожденная катаракта
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