Literature DB >> 31418098

Novel AKAP9 mutation and long QT syndrome in a patient with torsades des pointes.

Dario Bottigliero1, Ilenia Monaco1, Rosa Santacroce1, Grazia Casavecchia1, Michele Correale1, Francesca Guastafierro1, Angelica Leccese1, Giorgia Cordisco1, Riccardo Ieva2, Roberta Trunzo1, Matteo Di Biase3, Maurizio Margaglione1, Natale Daniele Brunetti4.   

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Year:  2019        PMID： 31418098     DOI： 10.1007/s10840-019-00606-y

Source DB:  PubMed          Journal:  J Interv Card Electrophysiol        ISSN： 1383-875X            Impact factor:   1.900


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  2 in total

1.  Mutation of an A-kinase-anchoring protein causes long-QT syndrome.

Authors:  Lei Chen; Michelle L Marquardt; David J Tester; Kevin J Sampson; Michael J Ackerman; Robert S Kass
Journal:  Proc Natl Acad Sci U S A       Date:  2007-12-19       Impact factor: 11.205

2.  AKAP9 is a genetic modifier of congenital long-QT syndrome type 1.

Authors:  Carin P de Villiers; Lize van der Merwe; Lia Crotti; Althea Goosen; Alfred L George; Peter J Schwartz; Paul A Brink; Johanna C Moolman-Smook; Valerie A Corfield
Journal:  Circ Cardiovasc Genet       Date:  2014-08-02
  2 in total

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