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A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
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A novel duplication confirms the involvement of 5q23.2 in autosomal dominant leukodystrophy

Inge A Meijer1, Ana A Simoes-Lopes, Sandra Laurent

  • 1Centre of Excellence in Neuromics, Centre Hospitalier de l'Université de Montreal and Ste-Justine Hospital, Montreal, Canada.

Archives of Neurology
|November 13, 2008
PubMed
Abstract

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