A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): Clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype-Reference-Cited by-同舟云学术

A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): Clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype

Published:2013-05-11 Issue:7 Volume:54 Page:1298-1306
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

Licchetta Laura¹,Pippucci Tommaso²,Bisulli Francesca¹,Cantalupo Gaetano³⁴,Magini Pamela²,Alvisi Lara¹,Baldassari Sara²,Martinelli Paolo¹,Naldi Ilaria¹,Vanni Nicola⁵,Liguori Rocco¹,Seri Marco²,Tinuper Paolo¹

Affiliation:

1. IRCCS Institute of Neurological Sciences of Bologna; Department of Biomedical and Neuromotor Sciences; University of Bologna; Bologna Italy

2. Medical Genetics Unit; Department of Gynaecological, Obstetric and Paediatric Sciences; Polyclinic Sant'Orsola-Malpighi; University of Bologna; Bologna Italy

3. Child Neuropsychiatry Unit; Department of Neuroscience; University-Hospital of Parma; Parma Italy

4. Department of Life and Reproduction Sciences; University of Verona; Verona Italy

5. Department of Neuroscience; Institute G. Gaslini; University of Genoa; Genoa Italy

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/epi.12216/fullpdf

Reference27 articles.

1. Merlin-rapid analysis of dense genetic maps using sparse gene flow trees;Abecasis;Nat Genet,2002

2. Natural history and long-term evolution in families with autosomal dominant cortical tremor, myoclonus, and epilepsy;Coppola;Epilepsia,2011