Identification of two new KCNA1 mutations in episodic ataxia/myokymia families

Abstract

Journal Article Identification of two new KCNA1 mutations in episodic ataxia/myokymia families Get access D.L. Browne, D.L. Browne 1Departments of Molecular and Medical Genetics Search for other works by this author on: Oxford Academic PubMed Google Scholar E.R.P. Brunt, E.R.P. Brunt 4Department of Neurology, University Hospital Groningen9700 RB Groningen The Netherlands Search for other works by this author on: Oxford Academic PubMed Google Scholar R.C. Griggs, R.C. Griggs 5Department of Neurology, University of Rochester Medical CenterRochester, NY 14642, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar J.G. Nutt, J.G. Nutt 3Departments of Neurology, Oregon Health Sciences UniversityPortland, OR 97201, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar S.T. Gancher, S.T. Gancher 3Departments of Neurology, Oregon Health Sciences UniversityPortland, OR 97201, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar E.A. Smith, E.A. Smith 1Departments of Molecular and Medical Genetics Search for other works by this author on: Oxford Academic PubMed Google Scholar M. Litt M. Litt * 1Departments of Molecular and Medical Genetics2Departments of Biochemistry and Molecular Biology *To whom correspondence should be addressed Search for other works by this author on: Oxford Academic PubMed Google Scholar Human Molecular Genetics, Volume 4, Issue 9, September 1995, Pages 1671–1672, https://doi.org/10.1093/hmg/4.9.1671 Published: 01 September 1995 Article history Received: 28 March 1995 Revision received: 25 May 1995 Accepted: 25 May 1995 Published: 01 September 1995