Mutational Analysis of Nicotinic Acetylcholine Receptor β2 Subunit Gene (CHRNB2) in a Representative Cohort of Italian Probands Affected by Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
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概要
- 論文の詳細を見る
- 2002-04-01
著者
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Tenchini Maria
Department Of Biology And Genetics For Medical Science University Of Milan
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DUGA Stefano
Department of Biology and Genetics for Medical Science, University of Milan
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ASSELTA Rosanna
Department of Biology and Genetics for Medical Science, University of Milan
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BONATI Maria
Department of Biology and Genetics for Medical Science, University of Milan
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MALCOVATI Massimo
Department of Biology and Genetics for Medical Science, University of Milan
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DALPRA Leda
Department of Experimenta and Environmental Medicine and Medical Biotechonology, University of Milan
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OLDANI Alessandro
Sleep Disorders Centre, Universita Vita-Salute, IRCCS H. San Raffaele
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ZUCCONI Marco
Sleep Disorders Centre, Universita Vita-Salute, IRCCS H. San Raffaele
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FERINI-STRAMBI Luigi
Sleep Disorders Centre, Universita Vita-Salute, IRCCS H. San Raffaele
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Zucconi Marco
Sleep Disorders Centre Universita Vita-salute Irccs H. San Raffaele
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Oldani Alessandro
Sleep Disorders Centre Universita Vita-salute Irccs H. San Raffaele
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Ferini-strambi Luigi
Sleep Disorders Centre Universita Vita-salute Irccs H. San Raffaele
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Dalpra Leda
Department Of Experimenta And Environmental Medicine And Medical Biotechonology University Of Milan-
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Duga Stefano
Department Of Biology And Genetics For Medical Science University Of Milan
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Bonati Maria
Department Of Biology And Genetics For Medical Science University Of Milan
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Malcovati Massimo
Department Of Biology And Genetics For Medical Science University Of Milan
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Asselta Rosanna
Department Of Biology And Genetics For Medical Science University Of Milan
関連論文
- Mutational Analysis of Nicotinic Acetylcholine Receptor β2 Subunit Gene (CHRNB2) in a Representative Cohort of Italian Probands Affected by Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
- Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms
- Letters to the Editor : REPLY
- Autosomal Dominant Nocturnal Frontal Lobe Epilepsy: Electroclinical Picture
- Characterisation of a non-recurrent familial translocation t(7;9)(q11.23;p24.3) points to a recurrent involvement of the Williams-Beuren syndrome region in chromosomal rearrangements