Volume 48, Issue 1, Pages (January 2013)

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Volume 48, Issue 1, Pages 63-66 (January 2013) Novel KCNQ2 Mutation in a Large Emirati Family With Benign Familial Neonatal Seizures Imad Y. Saadeldin, MD, Reham M. Milhem, MSc, Lihadh Al-Gazali, MBCHB, Bassam R. Ali, PhD Pediatric Neurology Volume 48, Issue 1, Pages 63-66 (January 2013) DOI: 10.1016/j.pediatrneurol.2012.09.012 Copyright © 2013 Elsevier Inc. Terms and Conditions

Figure 1 Pedigree illustrates four generations of a large Emirati family. Solid black symbols indicate individuals in the family who were diagnosed with a mutation or who demonstrated a history of seizures. Open symbols indicate healthy individuals. Pediatric Neurology 2013 48, 63-66DOI: (10.1016/j.pediatrneurol.2012.09.012) Copyright © 2013 Elsevier Inc. Terms and Conditions

Figure 2 Chromatograms of the proband (A) and the unaffected mother (B). The chromatograms reveal a deletion of an adenine nucleotide, c.1126_1127delA, in exon 9, resulting in a frameshift of the reading frame of the voltage-gated sensor Kv7.2 potassium channel. Pediatric Neurology 2013 48, 63-66DOI: (10.1016/j.pediatrneurol.2012.09.012) Copyright © 2013 Elsevier Inc. Terms and Conditions