Autosomal recessive deafness 1A (DFNB1A) in Yakut population isolate in Eastern Siberia : extensive accumulation of the splice site mutation IVS1+1G>A in GJB2 gene as a result of founder effect
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概要
- 論文の詳細を見る
- 2011-09-01
著者
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Posukh Olga
Laboratory Of Genetic Recombination And Segregation Institute Of Cytology And Genetics Siberian Branch Fine Russian Academy Of Sciences
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Dzhemileva Lilya
Department Of Genomlcs Institute Of Biochemistry And Genetics Ufa Scientific Centre Russian Academy Of Sciences
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Fedorova Sardana
Department Of Molecular Genetics Yakut Scientific Centre Of Complex Medical Problems Siberian Branch Of The Russian Academy Of Medical Sciences
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Khusnutdinova Elza
Department Of Molecular Genetics Yakut Scientific Centre Of Complex Medical Problems Siberian Branch Of The Russian Academy Of Medical Sciences
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BARASHKOV Nikolay
Department of Molecular Genetics, Yakut Scientific Centre of Complex Medical Problems, Siberian Branch of the Russian Academy of Medical Sciences
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TERYUTIN Fedor
Department of Molecular Genetics, Yakut Scientific Centre of Complex Medical Problems, Siberian Branch of the Russian Academy of Medical Sciences
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FEDOTOVA Elvira
Audiology-Logopaedic Center, Republican Hospital #1-National Medical Centre, Ministry of Public Health of the Sakha Republic
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LOBOV Simeon
Department of Genomlcs, Institute of Biochemistry and Genetics, Ufa Scientific Centre, Russian Academy of Sciences
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Teryutin Fedor
Department Of Molecular Genetics Yakut Scientific Centre Of Complex Medical Problems Siberian Branch Of The Russian Academy Of Medical Sciences
関連論文
- Autosomal recessive deafness 1A (DFNB1A) in Yakut population isolate in Eastern Siberia : extensive accumulation of the splice site mutation IVS1+1G>A in GJB2 gene as a result of founder effect
- Carrier frequency of GJB2 gene mutations c.35delG, c.235delC and c.167delT among the populations of Eurasia