TY  - GEN
AU  - Lal,Dennis
AU  - Pernhorst,Katharina
AU  - Klein,Karl Martin
AU  - Reif,Philipp
AU  - Tozzi,Rossana
AU  - Toliat,Mohammad R
AU  - Winterer,Georg
AU  - Neubauer,Bernd
AU  - Nürnberg,Peter
AU  - Rosenow,Felix
AU  - Becker,Felicitas
AU  - Lerche,Holger
AU  - Kunz,Wolfram S
AU  - Kurki,Mitja I
AU  - Hoffmann,Per
AU  - Becker,Albert J
AU  - Perucca,Emilio
AU  - Zara,Federico
AU  - Sander,Thomas
AU  - Weber,Yvonne G
TI  - Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy
SN  - 1528-1167
PY  - 2016///0429
KW  - Adolescent
KW  - Adult
KW  - Child
KW  - Child, Preschool
KW  - DNA Mutational Analysis
KW  - Epilepsies, Partial
KW  - genetics
KW  - Female
KW  - Genetic Predisposition to Disease
KW  - Humans
KW  - Male
KW  - Meta-Analysis as Topic
KW  - Middle Aged
KW  - Phenotype
KW  - RNA Splicing Factors
KW  - RNA-Binding Proteins
KW  - Sequence Deletion
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/epi.13076
ER  -