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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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Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to

C M Coffeen1, C E McKenna, A H Koeppen

  • 1Department of Human Genetics, University of Utah, Salt Lake City 84112, USA.

Human Molecular Genetics
|April 6, 2000
PubMed

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