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Updated: May 30, 2026

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
08:22

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 single base-pair deletion in the WFS1 gene causes Wolfram syndrome

Katherine Pitt1, Chela James, Inderpal S Kochar

  • 1Clinical and Molecular Genetics Unit, Developmental Endocrinology Research Group, Institute of Child Health, University College London and Great Ormond Street Hospital for Children NHS Trust, London, UK.

Journal of Pediatric Endocrinology & Metabolism : JPEM
|August 10, 2011
PubMed

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