Association of LOXL1 gene with Finnish exfoliation syndrome patients
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概要
- 論文の詳細を見る
- Nature Publishing Groupの論文
- 2009-05-01
著者
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Jarvela Irma
Department Of Medical Genetics University Of Helsinki
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Lemmela Susanna
Department Of Medical Genetics University Of Helsinki
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Heger Martin
Department Of Biosciences University Of Helsinki
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Eriksson Aldur
Department Of Genetic Epidemiology Folkhalsan Institute Of Genetics
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ONKAMO Paivi
Department of Biological and Environmental Sciences, University of Helsinki
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Onkamo Paivi
Department Of Biosciences University Of Helsinki
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Nurmi Hanna
Department Of Medical Genetics University Of Helsinki
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FORSMAN Eva
Department of Genetic Epidemiology, Folkhalsan Institute of Genetics
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LAIVUORI Hannele
Department of Medical Genetics, University of Helsinki
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KIVELA Tero
Department of Ophthalmology, University of Helsinki
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PUSKA Paivi
Department of Ophthalmology, University of Helsinki
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FORSIUS Henrik
Department of Genetic Epidemiology, Folkhalsan Institute of Genetics
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Puska Paivi
Department Of Ophthalmology University Of Helsinki
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Forsman Eva
Department Of Genetic Epidemiology Folkhalsan Institute Of Genetics
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Kivela Tero
Department Of Ophthalmology University Of Helsinki
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Laivuori Hannele
Department Of Medical Genetics University Of Helsinki
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Forsius Henrik
Department Of Genetic Epidemiology Folkhalsan Institute Of Genetics
関連論文
- Screening of BCS1L mutations in severe neonatal disorders suspicious for mitochondrial cause
- Association of the arginine vasopressin receptor 1A (AVPR1A) haplotypes with listening to music
- Association of LOXL1 gene with Finnish exfoliation syndrome patients