Article révisé par les pairs
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
MeSH keywords: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 générale: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:scp/84864928152
info:pmid/22863189
PMC3415540

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