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Long QT syndrome and left ventricular noncompaction in 4 family members across 2 generations with KCNQ1 mutation.
Kharbanda, Mira; Hunter, Amanda; Tennant, Stephen; Moore, David; Curtis, Stephanie; Hancox, Jules C; Murday, Victoria.
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  • Kharbanda M; West of Scotland Clinical Genetics Service, Level 2A Laboratory Medicine Building, Queen Elizabeth University Hospital, 1345 Govan Road, Glasgow, G51 4TF, UK. Electronic address: mira.kharbanda@nhs.net.
  • Hunter A; Royal Hospital for Children, 1345 Govan Road, Glasgow, G51 4TF, UK.
  • Tennant S; Department of Medical Genetics, Ashgrove House, Foresterhill, Aberdeen, AB25 2ZA, UK.
  • Moore D; Molecular Genetics, David Brock Building, Western General Hospital, Edinburgh, EH4 2XU, UK.
  • Curtis S; University Hospitals Bristol NHS Foundation Trust, Marlborough Street, Bristol, BS2 8HW, UK.
  • Hancox JC; School of Physiology, Pharmacology and Neuroscience, Biomedical Sciences Building, University Walk, Bristol, BS8 1TD, UK.
  • Murday V; West of Scotland Clinical Genetics Service, Level 2A Laboratory Medicine Building, Queen Elizabeth University Hospital, 1345 Govan Road, Glasgow, G51 4TF, UK.
Eur J Med Genet ; 60(5): 233-238, 2017 May.
Article en En | MEDLINE | ID: mdl-28249770
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome de QT Prolongado / Canal de Potasio KCNQ1 / Ventrículos Cardíacos / Mutación Límite: Female / Humans Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article
Texto completo
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome de QT Prolongado / Canal de Potasio KCNQ1 / Ventrículos Cardíacos / Mutación Límite: Female / Humans Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article