Literature DB >> 30375078

SCN5A variants in Brugada syndrome: True, true false, or false true.

Roddy Walsh1, Arthur A M Wilde1.   

Abstract

Entities:  

Keywords:  Brugada syndrome; SCN5A variants; genetic basis of Brugada syndrome

Mesh：

Substances：

Year:  2018        PMID： 30375078     DOI： 10.1111/jce.13774

Source DB:  PubMed          Journal:  J Cardiovasc Electrophysiol        ISSN： 1045-3873


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  3 in total

1.  Searching for genetic modulators of the phenotypic heterogeneity in Brugada syndrome.

Authors:  Laura Martínez-Campelo; Raquel Cruz; Alejandro Blanco-Verea; Isabel Moscoso; Eva Ramos-Luis; Ricardo Lage; María Álvarez-Barredo; María Sabater-Molina; Pablo Peñafiel-Verdú; Juan Jiménez-Jáimez; Moisés Rodríguez-Mañero; María Brion
Journal:  PLoS One       Date:  2022-03-01       Impact factor: 3.240

2.  Clinical impact of rare variants associated with inherited channelopathies: a 5-year update.

Authors:  Ramon Brugada; Oscar Campuzano; Georgia Sarquella-Brugada; Anna Fernandez-Falgueras; Sergi Cesar; Elena Arbelo; Mónica Coll; Alexandra Perez-Serra; Marta Puigmulé; Anna Iglesias; Mireia Alcalde; Marta Vallverdú-Prats; Victoria Fiol; Carles Ferrer-Costa; Bernat Del Olmo; Ferran Picó; Laura Lopez; Ana García-Alvarez; Paloma Jordà; Coloma Tiron de Llano; Rocío Toro; Simone Grassi; Antonio Oliva; Josep Brugada
Journal:  Hum Genet       Date:  2021-09-21       Impact factor: 5.881

Review 3.  Role of Non-Coding Variants in Brugada Syndrome.

Authors:  Adrian Pérez-Agustín; Mel Lina Pinsach-Abuin; Sara Pagans
Journal:  Int J Mol Sci       Date:  2020-11-13       Impact factor: 5.923
  3 in total

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