TY  - GEN
AU  - Soldovieri,Maria Virginia
AU  - Boutry-Kryza,Nadia
AU  - Milh,Mathieu
AU  - Doummar,Diane
AU  - Heron,Benedicte
AU  - Bourel,Emilie
AU  - Ambrosino,Paolo
AU  - Miceli,Francesco
AU  - De Maria,Michela
AU  - Dorison,Nathalie
AU  - Auvin,Stephane
AU  - Echenne,Bernard
AU  - Oertel,Julie
AU  - Riquet,Audrey
AU  - Lambert,Laetitia
AU  - Gerard,Marion
AU  - Roubergue,Anne
AU  - Calender,Alain
AU  - Mignot,Cyril
AU  - Taglialatela,Maurizio
AU  - Lesca,Gaetan
TI  - Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: first evidence for an altered channel regulation by syntaxin-1A
SN  - 1098-1004
PY  - 2014///1006
KW  - Animals
KW  - Biotinylation
KW  - CHO Cells
KW  - Cohort Studies
KW  - Cricetulus
KW  - Epilepsy, Benign Neonatal
KW  - genetics
KW  - Female
KW  - Gene Deletion
KW  - Germ-Line Mutation
KW  - Humans
KW  - KCNQ2 Potassium Channel
KW  - KCNQ3 Potassium Channel
KW  - Male
KW  - Mutagenesis, Insertional
KW  - Pedigree
KW  - Sequence Alignment
KW  - Syntaxin 1
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/humu.22500
ER  -