Masaryk University

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    2009

    1. Mutational Screening of SCN5A in Patients Suspected of LQTS
      RAUDENSKÁ, Martina, Tomáš NOVOTNÝ, Alexandra BITTNEROVÁ and Anna VAŠKŮ. Mutational Screening of SCN5A in Patients Suspected of LQTS. In European Journal of Heart Failure Supplements 2009; Vol. 8(2). 2009.
      More: https://is.muni.cz/publication/835823/en

    2008

    1. Mutation analysis of candidate genes SCN1B, KCND3 and ANK2 in patients with clinical diagnosis of Long QT syndrome.
      RAUDENSKÁ, Martina, Alexandra BITTNEROVÁ, Tomáš NOVOTNÝ, Alena FLORIÁNOVÁ, Karel CHROUST, Renata GAILLYOVÁ, Bořivoj SEMRÁD, Jitka KADLECOVÁ, Martina ŠIŠÁKOVÁ, Ondřej TOMAN and Jindřich ŠPINAR. Mutation analysis of candidate genes SCN1B, KCND3 and ANK2 in patients with clinical diagnosis of Long QT syndrome. Physiological Research. Praha: Akademie věd České republiky, 2008, 57/2008, No 6, p. 857-862. ISSN 1802-9973.
      More: https://is.muni.cz/publication/835826/en

    2007

    1. Mutational Screening of Human Genes which Are Associated with Long QT Syndrome Occurrence
      RAUDENSKÁ, Martina, Ivo PAPOUŠEK and Karel CHROUST. Mutational Screening of Human Genes which Are Associated with Long QT Syndrome Occurrence. In XI. setkání biochemiků a molekulárních biologů. Česká republika, Brno: Masarykova univerzita, 2007, p. 35-35. ISBN 978-80-210-4234-6.
      More: https://is.muni.cz/publication/835818/en
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