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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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Gitelman's syndrome (familial hypokalemia-hypomagnesemia)

A J Barakat1, O M Rennert

  • 1Department of Pediatrics and Nephrology, Georgetown University Medical Center, Washington, DC, USA. aybarakat@aol.com

Journal of Nephrology
|April 3, 2001
PubMed

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