TY  - GEN
AU  - Heron,Sarah E
AU  - Ong,Yeh Sze
AU  - Yendle,Simone C
AU  - McMahon,Jacinta M
AU  - Berkovic,Samuel F
AU  - Scheffer,Ingrid E
AU  - Dibbens,Leanne M
TI  - Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies
SN  - 1528-1167
PY  - 2013///0625
KW  - Age Factors
KW  - Cohort Studies
KW  - DNA Mutational Analysis
KW  - Female
KW  - Gene Frequency
KW  - Genetic Predisposition to Disease
KW  - genetics
KW  - Humans
KW  - Infant
KW  - Male
KW  - Membrane Proteins
KW  - Mutation
KW  - Nerve Tissue Proteins
KW  - Phenotype
KW  - Spasms, Infantile
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/epi.12167
ER  -