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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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LMNB1 mutation causes cerebellar involvement and a genome instability defect

José Luiz Pedroso1, Veridiana Munford2, André Uchimura Bastos2

  • 1Division of General Neurology and Ataxia Unit, Department of Neurology, Universidade Federal de São Paulo, São Paulo, SP, Brazil; Hospital Israelita Albert Einstein (HIAE), São Paulo, Brazil.

Journal of the Neurological Sciences
|July 19, 2017
PubMed
Summary

No abstract available in PubMed .

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