Titre :
  • Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy.
Auteur : Heinzen, Erin ; Depondt, Chantal ; Cavalleri, Gianpiero L ; Ruzzo, Elizabeth K ; Walley, Nicole M ; Need, Anna C ; Ge, Dongliang ; He, Min ; Cirulli, Elizabeth T ; Zhao, Qian ; Cronin, Kenneth D ; Gumbs, Curtis E ; Campbell, C Ryan ; Hong, Linda K ; Maia, Jessica M ; Shianna, Kevin V ; McCormack, Mark ; Radtke, Rodney A ; O'Conner, Gerard D ; Mikati, Mohamad A ; Gallentine, William B ; Husain, Aatif M ; Sinha, Saurabh R ; Chinthapalli, Krishna ; Puranam, Ram S ; McNamara, James O ; Ottman, Ruth ; Sisodiya, Sanjay M ; Delanty, Norman ; Goldstein, David B
Informations sur la publication : American journal of human genetics, 91, 2, (page 293-302)
Statut de publication : Publié, 2012-08
Sujet CREF : Sciences bio-médicales et agricoles
Mots-clés MeSH : Base Sequence
Epilepsy, Generalized -- genetics
European Continental Ancestry Group -- genetics
Exome -- genetics
Genetic Predisposition to Disease -- genetics
Genome-Wide Association Study
Genotype
Humans
Molecular Sequence Data
Sequence Alignment
Sequence Analysis, DNA
Note : Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
SCOPUS: ar.j
Langue :
  • Anglais
Identificateurs : urn:issn:0002-9297 
info:doi/10.1016/j.ajhg.2012.06.016
info:pii/S0002-9297(12)00325-4
info:pmid/22863189
info:pmcid/PMC3415540