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SCN1A duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis

SCN1A duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis

Carla Marini; Ingrid E. Scheffer; Rima Nabbout; Davide Mei; Kathy Cox; Leanne M. Dibbens; Jacinta M. McMahon; Xenia Iona; Rochio Sanchez Carpintero; Maurizio Elia; Maria Roberta Cilio; Nicola Specchio; Lucio Giordano; Pasquale Striano; Elena Gennaro; J. Helen Cross; Sara Kivity; Miriam Y. Neufeld; Zaid Afawi; Eva Andermann; Daniel Keene; Olivier Dulac; Federico Zara; Samuel F. Berkovic; Renzo Guerrini; John C. Mulley
  • 作者Carla Marini; Ingrid E. Scheffer; Rima Nabbout; Davide Mei; Kathy Cox; Leanne M. Dibbens; Jacinta M. McMahon; Xenia Iona; Rochio Sanchez Carpintero; Maurizio Elia; Maria Roberta Cilio; Nicola Specchio; Lucio Giordano; Pasquale Striano; Elena Gennaro; J. Helen Cross; Sara Kivity; Miriam Y. Neufeld; Zaid Afawi; Eva Andermann; Daniel Keene; Olivier Dulac; Federico Zara; Samuel F. Berkovic; Renzo Guerrini; John C. Mulley
  • 卷第50卷
  • 期第7期
  • 印刷ISSN1528-1167
  • 文件大小178.19KB
  • 发表时间2009
  • DOI10.1111/j.1528-1167.2009.02013.x
  • 页码1670-1678
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