Mapping of a Locus for a Familial Autosomal Recessive Idiopathic Myoclonic Epilepsy of Infancy to Chromosome 16p13 Federico Zara, Elena Gennaro, Mariano.

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Mapping of a Locus for a Familial Autosomal Recessive Idiopathic Myoclonic Epilepsy of Infancy to Chromosome 16p13 Federico Zara, Elena Gennaro, Mariano Stabile, Ilaria Carbone, Michela Malacarne, Luigi Majello, Roberto Santangelo, Fabrizio Antonio de Falco, Franca Dagna Bricarelli The American Journal of Human Genetics Volume 66, Issue 5, Pages 1552-1557 (May 2000) DOI: 10.1086/302876 Copyright © 2000 The American Society of Human Genetics Terms and Conditions

Figure 1 Pedigree and chromosome 16p13 haplotypes of the Italian family segregating idiopathic myoclonic epilepsy of infancy. Filled symbols, affected subjects; unfilled symbols, individuals with no history of seizures. Individuals IV-6 and IV-22 had GTCSs and febrile convulsion, respectively. Individuals III-8, III-13 and III-14 did not consented to the study. Arrows, key recombinations that define the critical region. The American Journal of Human Genetics 2000 66, 1552-1557DOI: (10.1086/302876) Copyright © 2000 The American Society of Human Genetics Terms and Conditions

Figure 2 Genetic map of chromosome 16p13 markers. Order of markers and distances are taken from the Généthon map. Markers harboring the critical region are indicated in bold. The American Journal of Human Genetics 2000 66, 1552-1557DOI: (10.1086/302876) Copyright © 2000 The American Society of Human Genetics Terms and Conditions