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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 Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

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Molecular defects in Sanfilippo syndrome type B (mucopolysaccharidosis IIIB)

C E Beesley1, M Jackson, E P Young

  • 1Biochemistry, Endocrinology and Metabolism Unit, Institute of Child Health, University College London, London, UK. C.Beesley@ich.ucl.ac.uk

Journal of Inherited Metabolic Disease
|September 10, 2005
PubMed

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