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Mutation analysis of candidate genes SCN1B, KCND3 and ANK2 in patients with clinical diagnosis of long QT syndrome.
Raudenská, M; Bittnerová, A; Novotný, T; Floriánová, A; Chroust, K; Gaillyová, R; Semrád, B; Kadlecová, J; Sisáková, M; Toman, O; Spinar, J.
Affiliation
  • Raudenská M; Department of Genetics and Molecular Biology, Faculty of Science, Masaryk University, Brno, Czech Republic.
Physiol Res ; 57(6): 857-862, 2008.
Article in En | MEDLINE | ID: mdl-18052691
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Collection: 01-internacional Database: MEDLINE Main subject: Long QT Syndrome / DNA Mutational Analysis / Sodium Channels / Ankyrins / Shal Potassium Channels / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Female / Humans / Male / Middle aged Language: En Journal: Physiol Res Journal subject: FISIOLOGIA Year: 2008 Document type: Article Affiliation country: República Checa Country of publication: República Checa
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Long QT Syndrome / DNA Mutational Analysis / Sodium Channels / Ankyrins / Shal Potassium Channels / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Female / Humans / Male / Middle aged Language: En Journal: Physiol Res Journal subject: FISIOLOGIA Year: 2008 Document type: Article Affiliation country: República Checa Country of publication: República Checa