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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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Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma

B E Baysal1, R E Ferrell, J E Willett-Brozick

  • 1Department of Psychiatry, The University of Pittsburgh Medical Center, Pittsburgh, PA 15213-2593, USA. baysalbe@msx.upmc.edu

Science (New York, N.Y.)
|February 5, 2000
PubMed

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