Proposed genetic classification of the "benign" familial neonatal and infantile epilepsies

Epilepsia. 2011 Mar;52(3):649-50. doi: 10.1111/j.1528-1167.2010.02953.x.

Authors

John C Mulley¹, Sarah E Heron, Leanne M Dibbens

Affiliation

¹ Department of Genetic Medicine, Directorate of Genetics and Molecular Pathology, SA Pathology at Women's and Children's Hospital, Adelaide, Australia.

PMID: 21395569
DOI: 10.1111/j.1528-1167.2010.02953.x

No abstract available

Publication types

Comment
Research Support, Non-U.S. Gov't

MeSH terms

Age Factors
Age of Onset
Epilepsy, Benign Neonatal / classification*
Epilepsy, Benign Neonatal / diagnosis
Epilepsy, Benign Neonatal / genetics*
Genetic Variation / genetics
Genotype
Humans
Infant
Infant, Newborn
KCNQ1 Potassium Channel / genetics
KCNQ3 Potassium Channel / genetics
NAV1.2 Voltage-Gated Sodium Channel
Nerve Tissue Proteins / genetics
Sodium Channels / genetics
Terminology as Topic

Substances

KCNQ1 Potassium Channel
KCNQ3 Potassium Channel
KCNQ3 protein, human
NAV1.2 Voltage-Gated Sodium Channel
Nerve Tissue Proteins
SCN2A protein, human
Sodium Channels