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Benign Familial Infantile Convulsions: Linkage to Chromosome 16p12-q12 in 14 Families

✍ Scribed by Yvonne G. Weber; Andrea Berger; Nerses Bebek; Sabine Maier; Skevos Karafyllakes; Nancy Meyer; Yukio Fukuyama; Anne Halbach; Christiane Hikel; Gerhard Kurlemann; Bernd Neubauer; Makiko Osawa; Burkhard Püst; Dietz Rating; Kayoko Saito; Ulrich Stephani; Ulrike Tauer; Frank Lehmann-Horn; Karin Jurkat-Rott; Holger Lerche


Book ID
110726798
Publisher
Wiley (Blackwell Publishing)
Year
2004
Tongue
English
Weight
316 KB
Volume
45
Category
Article
ISSN
0013-9580

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## Abstract Juvenile myoclonic epilepsy is a common subtype of idiopathic epilepsy accounting for 4–11% of all epilepsies. We reported previously significant evidence of linkage between chromosome 6p12–11 microsatellites and the clinical epilepsy and EEG traits of JME families from Belize and Los A