Reference : KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expa...
Scientific journals : Article
Life sciences : Genetics & genetic processes
http://hdl.handle.net/2268/102173
KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum.
English
Singh, Nanda A [> > > >]
Westenskow, Peter [> > > >]
Charlier, Carole mailto [> > > >]
Pappas, Chris [> > > >]
Leslie, Jonathan [> > > >]
Dillon, Jessica [> > > >]
Anderson, V Elving [> > > >]
Sanguinetti, Michael C [> > > >]
Leppert, Mark F [ > > ]
2003
Brain : A Journal of Neurology
Oxford University Press
126
Pt 12
2726-37
Yes (verified by ORBi)
International
0006-8950
1460-2156
Oxford
United Kingdom
[en] Animals ; DNA Mutational Analysis/methods ; Epilepsy, Benign Neonatal/genetics ; Gene Deletion ; Humans ; Infant, Newborn ; KCNQ2 Potassium Channel ; KCNQ3 Potassium Channel ; Mutation ; Oocytes/metabolism ; Patch-Clamp Techniques ; Pedigree ; Potassium Channels/genetics/physiology ; Potassium Channels, Voltage-Gated ; RNA, Complementary/genetics ; Transcription, Genetic ; Xenopus laevis
[en] Benign familial neonatal convulsions (BFNC) is a rare autosomal dominant generalized epilepsy of the newborn infant. Seizures occur repeatedly in the first days of life and remit by approximately 4 months of age. Previously our laboratory cloned two novel potassium channel genes, KCNQ2 and KCNQ3, and showed that they are mutated in patients with BFNC. In this report, we characterize the breakpoints of a previously reported interstitial deletion in the KCNQ2 gene and show that only KCNQ2 is deleted. We identify 11 novel mutations in KCNQ2 and one novel mutation in the KCNQ3 potassium channel genes. In one family, the phenotype extends beyond neonatal seizures and includes rolandic seizures, and a subset of families has onset of seizures in infancy. In the Xenopus oocyte expression system, we characterize five KCNQ2 and one KCNQ3 disease-causing mutations. These mutations cause a variable loss of function, and selective effects on the biophysical properties of KCNQ2/KCNQ3 heteromultimeric channels. We report here the first dominant negative mutation in KCNQ2 that has a phenotype of neonatal seizures without permanent clinical CNS impairment.
http://hdl.handle.net/2268/102173
10.1093/brain/awg286

File(s) associated to this reference

Fulltext file(s):

FileCommentaryVersionSizeAccess
Restricted access
Brain-2003-Singh-2726-37.pdfPublisher postprint485.64 kBRequest copy

Bookmark and Share SFX Query

All documents in ORBi are protected by a user license.