Screening of BCS1L mutations in severe neonatal disorders suspicious for mitochondrial cause
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概要
- 論文の詳細を見る
- 2008-06-01
著者
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FELLMAN Vineta
Hospital for Children and Adolescents, Helsinki University Central Hospital
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LEMMELA Susanna
Department of Medical Genetics, University of Helsinki
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SAJANTILA Antti
Department of Forensic Medicine, University of Helsinki
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PIHKO Helena
Hospital for Children and Adolescents, Helsinki University Central Hospital
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JARVELA Irma
Department of Medical Genetics, University of Helsinki
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Jarvela Irma
Department Of Medical Genetics University Of Helsinki
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Pihko Helena
Hospital For Children And Adolescents Helsinki University Central Hospital
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Fellman Vineta
Hospital For Children And Adolescents Helsinki University Central Hospital
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Sajantila Antti
Department Of Forensic Medicine University Of Helsinki
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Lemmela Susanna
Department Of Medical Genetics University Of Helsinki
関連論文
- Screening of BCS1L mutations in severe neonatal disorders suspicious for mitochondrial cause
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