Late-onset and Slow-progressing Lafora Disease in Four Siblings with EPM2B Mutation
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概要
- 論文の詳細を見る
- 2005-10-01
著者
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BEBEK Nerses
Department of Neurology, Istanbul faculty of Medicine
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GURSES Candan
Department of Neurology, Istanbul faculty of Medicine
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BAYKAN Betul
Department of Neurology, Instanbul faculty of Medicine
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GIANOTTI Stefania
Laboratory of Human Genetics, E. O.
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ZARA Federico
Laboratory of Neurogenetics, Unit of Neuromuscular Disease, Gaslini Institute and University of Geno
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GENNARO Elena
Laboratory of Human Genetics, E.O. Ospedali Galliera
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Gianotti Stefania
Laboratory Of Human Genetics E. O.
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Striano Pasquale
Epilepsy Center Department Of Neurological Sciences Federico Ii University
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Bebek Nerses
Department Of Neurology Istanbul Faculty Of Medicine
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Bebek Nerses
Department Of Applied Physiology University Of Ulm
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Gennaro Elena
Laboratory Of Human Genetics E.o. Ospedali Galliera
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Zara Federico
Laboratory Of Neurogenetics Department Of Muscular And Neurodegenerative Disease "g. Gaslini&qu
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Gurses Candan
Department Of Neurology Istanbul Faculty Of Medicine
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Zara Federico
Laboratory Of Neurogenetics Unit Of Neuromuscular Disease Gaslini Institute And University Of Genova
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Baykan Betul
Department Of Neurology Instanbul Faculty Of Medicine
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Striano Pasquale
Epilepsy Center Federico Ii University
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- Electroclinical and Genetic Findings in a Family with Cortical Tremor, Myoclonus, and Epilepsy
- Late-onset and Slow-progressing Lafora Disease in Four Siblings with EPM2B Mutation
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