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Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the α 1 subunit of the inhibitory glycine receptor

1994; Oxford University Press; Volume: 3; Issue: 12 Linguagem: Inglês

10.1093/hmg/3.12.2175

1460-2083

Mark I. Rees, Martin Andrew, Sudad Jawad, Michael J. Owen,

Mitochondrial Function and Pathology

Journal Article Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the α1 subunit of the inhibitory glycine receptor Get access Mark I. Rees, Mark I. Rees 1Departments of Psychological Medicine, University of Wales College of MedicineHealth Park, Cardiff CF4, 4XN, UK2Medical Genetics, University of Wales College of MedicineHealth Park, Cardiff CF4 4XN, UK Search for other works by this author on: Oxford Academic PubMed Google Scholar Martin Andrew, Martin Andrew 1Departments of Psychological Medicine, University of Wales College of MedicineHealth Park, Cardiff CF4, 4XN, UK Search for other works by this author on: Oxford Academic PubMed Google Scholar Sudad Jawad, Sudad Jawad 1Departments of Psychological Medicine, University of Wales College of MedicineHealth Park, Cardiff CF4, 4XN, UK Search for other works by this author on: Oxford Academic PubMed Google Scholar Michael J. Owen Michael J. Owen 1Departments of Psychological Medicine, University of Wales College of MedicineHealth Park, Cardiff CF4, 4XN, UK2Medical Genetics, University of Wales College of MedicineHealth Park, Cardiff CF4 4XN, UK Search for other works by this author on: Oxford Academic PubMed Google Scholar Human Molecular Genetics, Volume 3, Issue 12, December 1994, Pages 2175–2179, https://doi.org/10.1093/hmg/3.12.2175 Published: 01 December 1994 Article history Received: 01 August 1994 Accepted: 16 September 1994 Published: 01 December 1994