Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2 (original) (raw)
- Brief Communication
- Published: April 2000
- Bryan T. MacDonald1,8,
- Miriam H. Meisler1,8,
- Stéphanie Baulac2,9 na1,
- Gilles Huberfeld2,9,
- Isabelle An-Gourfinkel3,4,9,
- Alexis Brice2,5,9,
- Eric LeGuern2,9,
- Bruno Moulard6,10 na1,
- Denys Chaigne7,10 na1,
- Catherine Buresi6,10 na1 &
- …
- Alain Malafosse6,10 na1
Nature Genetics volume 24, pages 343–345 (2000)Cite this article
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Abstract
Generalized epilepsy with febrile seizures plus type 2 (GEFS+2, MIM 604233) is an autosomal dominant disorder characterized by febrile seizures in children and afebrile seizures in adults. We describe here two mutations of the gene encoding the neuronal voltage-gated sodium channel (SCN1A), Thr875Met and Arg1648His, that co-segregate with the disorder in two families with GEFS+ linked to chromosome 2q. These mutations identify a new disease gene for human inherited epilepsy.
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References
- Scheffer, I.E. & Berkovic, S.F. Brain 120, 479–490 (1997).
Article Google Scholar - Wallace, R.H. et al. Nature Genet. 19, 366–370 (1998).
Article CAS Google Scholar - Moulard, B. et al. Am. J. Hum. Genet. 65, 1396–1400 (1999).
Article CAS Google Scholar - Baulac, S. et al. Am. J. Hum. Genet. 65, 1078–1085 (1999).
Article CAS Google Scholar - Plummer, N. & Meisler, M.H. Genomics 57, 323–331 (1999).
Article CAS Google Scholar - Noda, M. & Numa, S. J. Recept. Res. 7, 467–497 (1987).
Article CAS Google Scholar - Smith, R.D. & Goldin, A.L. J. Neurosci. 18, 811–820 (1998).
Article CAS Google Scholar - Escayg, A. et al. Am. J. Hum. Genet. (in press).
- Kühn, F.J.P. & Greeff, N.G. J. Gen. Physiol. 114, 167–183 (1999).
Article Google Scholar - Bulman, D.E. Hum. Mol. Genet. 6, 1679–1685 (1997).
Article CAS Google Scholar - Lehmann-Horn, F. & Jurkat-Rott, K. Physiol. Rev. 79, 1317–1372 (1999).
Article CAS Google Scholar - Wattanasirichaigoon, D. et al. Am. J. Med. Genet. 86, 470–476 (1999).
Article CAS Google Scholar - Catterall, W.A. Adv. Neurol. 79, 441–456 (1999).
CAS PubMed Google Scholar - Peiffer, A. et al. Ann. Neurol. 46, 671–678 (1999).
Article CAS Google Scholar - Lopes-Cendes, I.E. et al. Am. J. Hum. Genet. 66, 698–701 (2000).
Article CAS Google Scholar
Acknowledgements
We thank L. Isom and L.K. Sprunger for helpful discussions, and F. Picard and J.-F. Prudhomme for participation in identification of family 2. This research was supported by NIH Grant NS34509 (Group 1), the Association pour le Développement de la Recherche sur les Maladies Génétiques Neurologiques et Psychiatriques (ADRMGNP) (Group 2) and the Swiss National Science Foundation (Group 3).
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Author notes
- Andrew Escayg, Stéphanie Baulac, Bruno Moulard, Denys Chaigne, Catherine Buresi and Alain Malafosse: These authors contributed equally to this work.
Authors and Affiliations
- Department of Human Genetics, University of Michigan, Ann Arbor, Michigan, USA
Andrew Escayg, Bryan T. MacDonald & Miriam H. Meisler - INSERM U289, Hôpital de la Salpêtrière, Paris, France
Stéphanie Baulac, Gilles Huberfeld, Alexis Brice & Eric LeGuern - Centre d'Epilepsie, Hôpital de la Salpêtrière, Paris, France
Isabelle An-Gourfinkel - Généthon, Evry, France
Isabelle An-Gourfinkel - Consultation de Génétique Médicale, Hôpital de la Salpêtrière, Paris, France
Alexis Brice - Division de Neuropsychiatrie, Hôpitaux Universitaires de Genève, Chêne-Bourg, Switzerland
Bruno Moulard, Catherine Buresi & Alain Malafosse - Clinique Sainte-Odile, Strasbourg, France
Denys Chaigne - Group 1,
Andrew Escayg, Bryan T. MacDonald & Miriam H. Meisler - Group 2,
Stéphanie Baulac, Gilles Huberfeld, Isabelle An-Gourfinkel, Alexis Brice & Eric LeGuern - Group 3,
Bruno Moulard, Denys Chaigne, Catherine Buresi & Alain Malafosse
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- Andrew Escayg
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Correspondence toMiriam H. Meisler.
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Escayg, A., MacDonald, B., Meisler, M. et al. Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.Nat Genet 24, 343–345 (2000). https://doi.org/10.1038/74159
- Issue Date: April 2000
- DOI: https://doi.org/10.1038/74159