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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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[Wolfram syndrome: clinical and genetic analysis in two sisters]

J-B Conart1, T Maalouf, P Jonveaux

  • 1Service d'ophtalmologie B, CHU de Nancy, allée du Morvan, 54511 Vandoeuvre-les-Nancy cedex, France.

Journal Francais D'Ophtalmologie
|June 3, 2011
PubMed

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