NURMI Hanna | Department of Medical Genetics, University of Helsinki

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• NURMI Hannaの詳細を見る
• 同名の論文著者
• Department of Medical Genetics, University of Helsinkiの論文著者

Department of Medical Genetics, University of Helsinki | 論文

• Screening of BCS1L mutations in severe neonatal disorders suspicious for mitochondrial cause
• Familial Unverricht-Lundborg Disease: A Clinical, Neurophysiologic, and Genetic Study
• Association of LOXL1 gene with Finnish exfoliation syndrome patients

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