Literature DB >> 11530094

LQT genotype-phenotype relationships: patients and patches.

A A Wilde, D Escande.   

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Year:  2001        PMID： 11530094     DOI： 10.1016/s0008-6363(01)00389-3

Source DB:  PubMed          Journal:  Cardiovasc Res        ISSN： 0008-6363            Impact factor:   10.787


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  2 in total

1.  Stop-codon and C-terminal nonsense mutations are associated with a lower risk of cardiac events in patients with long QT syndrome type 1.

Authors:  Martin H Ruwald; Xiaorong Xu Parks; Arthur J Moss; Wojciech Zareba; Jayson Baman; Scott McNitt; Jorgen K Kanters; Wataru Shimizu; Arthur A Wilde; Christian Jons; Coeli M Lopes
Journal:  Heart Rhythm       Date:  2015-08-28       Impact factor: 6.343

2.  Phenotype, origin and estimated prevalence of a common long QT syndrome mutation: a clinical, genealogical and molecular genetics study including Swedish R518X/KCNQ1 families.

Authors:  Annika Winbo; Eva-Lena Stattin; Charlotte Nordin; Ulla-Britt Diamant; Johan Persson; Steen M Jensen; Annika Rydberg
Journal:  BMC Cardiovasc Disord       Date:  2014-02-19       Impact factor: 2.298
  2 in total

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