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ESP028 Myoclonic epilepsy in a child with deletion 15q26.1-26.2

✍ Scribed by C. Veredice; D. Battaglia; I. Contaldo; F. Bianco; M.C. Stefanini; D. Lettori; G. Vasco; M. Zollino; F. Guzzetta

Book ID
114359701
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
54 KB
Volume
11
Category
Article
ISSN
1090-3798

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## Abstract Neuroligin 1 (__NLGN1__) is one of five members of the neuroligin gene family and may represent a candidate gene for neurological disorders, as members of this family are involved in formation and remodeling of central nervous system synapses. __NLGN1__ is expressed predominantly in the