Are GJB2 mutations an aggravating factor in the phenotypic expression of mitochondrial non-syndromic deafness?
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概要
- 論文の詳細を見る
- Nature Publishing Groupの論文
- 2010-05-01
著者
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KANDILOROS Dimitrios
Department Otorhinolaryngology The Athens National University
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Petersen Michael
Department Of Genetics Institute Of Child Health 'aghia Sophia' Children's Hospital
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KOKOTAS Haris
Department of Genetics, Institute of Child Health, 'Aghia Sophia' Children's Hospital
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GRIGORIADOU Maria
Department of Genetics, Institute of Child Health, 'Aghia Sophia' Children's Hospital
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KORRES George
Department of Genetics, Institute of Child Health, 'Aghia Sophia' Children's Hospital
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FEREKIDOU Elisabeth
Department of Genetics, Institute of Child Health, 'Aghia Sophia' Children's Hospital
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GIANNOULIA-KARANTANA Aglaia
Department of Pediatrics, Athens University Medical School, "Aghia Sophia' Children's Hospital
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KORRES Stavros
Department of Otorhinolaryngology-Head and Neck Surgery, Athens University Medical School, Hippokration Hospital
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Korres George
Department Of Genetics Institute Of Child Health 'aghia Sophia' Children's Hospital
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Kokotas Haris
Department Of Genetics Institute Of Child Health 'aghia Sophia' Children's Hospital
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Giannoulia-karantana Aglaia
Department Of Pediatrics Athens University Medical School "aghia Sophia' Children's Hospital
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Ferekidou Elisabeth
Department Of Genetics Institute Of Child Health 'aghia Sophia' Children's Hospital
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Grigoriadou Maria
Department Of Genetics Institute Of Child Health 'aghia Sophia' Children's Hospital
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Korres Stavros
Department Of Otorhinolaryngology-head And Neck Surgery Athens University Medical School Hippokration Hospital
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KANDILOROS Dimitrios
Department of Otorhinolaryngology-Head and Neck Surgery, Athens University Medical School, Hippokration Hospital
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- Are GJB2 mutations an aggravating factor in the phenotypic expression of mitochondrial non-syndromic deafness?
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