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Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders.
Heyes, Samuel; Pratt, Wendy S; Rees, Elliott; Dahimene, Shehrazade; Ferron, Laurent; Owen, Michael J; Dolphin, Annette C.
Afiliación
  • Heyes S; Department of Neuroscience, Physiology and Pharmacology, University College London, London WC1E 6BT, UK.
  • Pratt WS; Department of Neuroscience, Physiology and Pharmacology, University College London, London WC1E 6BT, UK.
  • Rees E; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Neuroscience and Mental Health Research Institute, Institute of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff CF24 4HQ, UK.
  • Dahimene S; Department of Neuroscience, Physiology and Pharmacology, University College London, London WC1E 6BT, UK.
  • Ferron L; Department of Neuroscience, Physiology and Pharmacology, University College London, London WC1E 6BT, UK.
  • Owen MJ; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Neuroscience and Mental Health Research Institute, Institute of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff CF24 4HQ, UK.
  • Dolphin AC; Department of Neuroscience, Physiology and Pharmacology, University College London, London WC1E 6BT, UK. Electronic address: a.dolphin@ucl.ac.uk.
Prog Neurobiol ; 134: 36-54, 2015 Nov.
Article en En | MEDLINE | ID: mdl-26386135
This review summarises genetic studies in which calcium channel genes have been connected to the spectrum of neuropsychiatric syndromes, from bipolar disorder and schizophrenia to autism spectrum disorders and intellectual impairment. Among many other genes, striking numbers of the calcium channel gene superfamily have been implicated in the aetiology of these diseases by various DNA analysis techniques. We will discuss how these relate to the known monogenic disorders associated with point mutations in calcium channels. We will then examine the functional evidence for a causative link between these mutations or single nucleotide polymorphisms and the disease processes. A major challenge for the future will be to translate the expanding psychiatric genetic findings into altered physiological function, involvement in the wider pathology of the diseases, and what potential that provides for personalised and stratified treatment options for patients.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Canales de Calcio / Trastornos Mentales / Enfermedades del Sistema Nervioso Tipo de estudio: Diagnostic_studies Límite: Animals / Humans Idioma: En Revista: Prog Neurobiol Año: 2015 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Canales de Calcio / Trastornos Mentales / Enfermedades del Sistema Nervioso Tipo de estudio: Diagnostic_studies Límite: Animals / Humans Idioma: En Revista: Prog Neurobiol Año: 2015 Tipo del documento: Article