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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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Zellweger syndrome and associated brain malformations: report of a novel Peroxin1 (PEX1) mutation in a Native

Mohammad R Mohebbi1, Eric T Rush, William B Rizzo

  • 1Siouxland Medical Education Foundation-University of Iowa, Sioux City, IA 51104, USA. mrmohebbi@yahoo.com

Journal of Child Neurology
|March 2, 2012
PubMed

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