Different electroclinical picture of generalized epilepsy in two families with 15q13.3 microdeletion-Reference-Cited by-同舟云学术

Different electroclinical picture of generalized epilepsy in two families with 15q13.3 microdeletion

Published:2013-02-28 Issue:5 Volume:54 Page:e69-e73
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

Coppola Antonietta,Bagnasco Irene¹,Traverso Monica²,Brusco Alfredo³,Di Gregorio Eleonora³,Del Gaudio Luigi⁴,Santulli Lia⁴,Caccavale Carmela⁴,Vigliano Piernanda¹,Minetti Carlo⁵,Striano Salvatore⁴,Zara Federico²,Striano Pasquale⁵

Affiliation:

1. Neuropsychiatric Unit; Martini Ovest Hospital; Turin; Italy

2. Laboratory of Neurogenetics; G. Gaslini Institute; Genova; Italy

3. Department of Genetics Biology and Biochemistry; University of Turin; S.C.d.U. Medical Genetics; A.O.U. San Giovanni Battista; Turin; Italy

4. Epilepsy Center; Neurology Department; Federico II University of Naples; Naples; Italy

5. Pediatric Neurology and Muscular Diseases Unit; Department of Neurosciences-DINOGMI; Gaslini Institute; Genova; Italy

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/epi.12130/fullpdf

Reference12 articles.

1. Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders;Ben-Shachar;J Med Genet,2009

2. Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance;Dibbens;Hum Mol Genet,2009

3. Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes;Heinzen;Am J Hum Genet,2010

4. 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy;Helbig;Nat Genet,2009

5. Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders;Miller;J Med Genet,2009

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