A novel CAG repeat configuration in the <i>SCA1</i> gene: implications for the molecular diagnostics of spinocerebellar ataxia type 1

Abstract

Journal Article A novel CAG repeat configuration in the SCA1 gene: implications for the molecular diagnostics of spinocerebellar ataxia type 1 Get access Franklin Quan, Franklin Quan 1DNA Diagnostic LaboratoryPortland OR 97201, USA2Department of Molecular and Medical GeneticsPortland OR 97201, USA4Shriners Hospital for Crippled ChildrenPortland OR 97201, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar Joanne Janas, Joanne Janas 3Department of Neurology, Division of Pediatric Neurology, Oregon Health Sciences UniversityPortland OR 97201, USA4Shriners Hospital for Crippled ChildrenPortland OR 97201, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar Bradley W. Popovich Bradley W. Popovich * 1DNA Diagnostic LaboratoryPortland OR 97201, USA2Department of Molecular and Medical GeneticsPortland OR 97201, USA4Shriners Hospital for Crippled ChildrenPortland OR 97201, USA *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 12, December 1995, Pages 2411–2413, https://doi.org/10.1093/hmg/4.12.2411 Published: 01 December 1995 Article history Received: 20 July 1995 Revision received: 23 September 1995 Accepted: 23 September 1995 Published: 01 December 1995