Evidence for S284L Mutation of the CHRNA4 in a White Family with Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
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概要
- 論文の詳細を見る
- 2003-08-01
著者
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Trzeciak Wieslaw
Department Of Biochemistry And Molecular Biology University Of Medical Sciences
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ROZYCKA Agata
Department of Biochemistry and Molecular Biology, University of Medical Sciences
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SKORUPSKA Elzbieta
Department of Biochemistry and Molecular Biology, University of Medical Sciences
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KOSTYRKO Andrzej
Department of Biochemistry and Molecular Biology, University of Medical Sciences
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Rozycka Agata
Department Of Biochemistry And Molecular Biology University Of Medical Sciences
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Kostyrko Andrzej
Department Of Biochemistry And Molecular Biology University Of Medical Sciences
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Skorupska Elzbieta
Department Of Biochemistry And Molecular Biology University Of Medical Sciences
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- Substitution of M398T in the Second Transmembrane Helix of the LH Receptor in a Patient with Familial Male-Limited Precocious Puberty
- Evidence for S284L Mutation of the CHRNA4 in a White Family with Autosomal Dominant Nocturnal Frontal Lobe Epilepsy