Figure 3, Segregation analysis of the PCDH19 deletion and point mutations in 12 families - Jasper's Basic Mechanisms of the Epilepsies

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Noebels JL, Avoli M, Rogawski MA, et al., editors. Jasper's Basic Mechanisms of the Epilepsies [Internet]. 4th edition. Bethesda (MD): National Center for Biotechnology Information (US); 2012.

This title is an author manuscript version first made accessible on the NCBI Bookshelf website July 2, 2012.

This title is an author manuscript version first made accessible on the NCBI Bookshelf website July 2, 2012.

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Jasper's Basic Mechanisms of the Epilepsies [Internet]. 4th edition.

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Figure 3Segregation analysis of the PCDH19 deletion and point mutations in 12 families

del/+, m/+ and v/+ denote individuals heterozygous for the deletion, mutation or variant, respectively; +/+ denotes individuals carrying homozygous wild-type alleles. Squares represent males, circles females; filled black symbols: patients diagnosed as having Dravet syndrome; right black half: Cognitive delay or impairment; left gray half: adolescence-onset idiopathic epilepsy. Dots in the middle of the squares indicate unaffected mutation carriers. The arrows indicate the index cases (from Depienne et al., 2009).⁵⁹

From: Genes in infantile epileptic encephalopathies

All Jasper's Basic Mechanisms of the Epilepsies content, except where otherwise noted, is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported license, which permits copying, distribution and transmission of the work, provided the original work is properly cited, not used for commercial purposes, nor is altered or transformed.

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Depienne C, Gourfinkel-An I, Baulac S, et al. Genes in infantile epileptic encephalopathies. In: Noebels JL, Avoli M, Rogawski MA, et al., editors. Jasper's Basic Mechanisms of the Epilepsies [Internet]. 4th edition. Bethesda (MD): National Center for Biotechnology Information (US); 2012. Figure 3, Segregation analysis of the PCDH19 deletion and point mutations in 12 families.
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Jasper's Basic Mechanisms of the Epilepsies [Internet]. 4th edition.

Figure 3Segregation analysis of the PCDH19 deletion and point mutations in 12 families

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