Literature DB >> 32164423

Established Loss-of-Function Variants in ANK2-Encoded Ankyrin-B Rarely Cause a Concerning Cardiac Phenotype in Humans.

John R Giudicessi1, Michael J Ackerman2,3,4.   

Abstract

Entities:  

Keywords:  ankyrin; death, sudden; exome; human; mice; phenotype

Mesh：

Substances：

Year:  2020        PMID： 32164423     DOI： 10.1161/CIRCGEN.119.002851

Source DB:  PubMed          Journal:  Circ Genom Precis Med        ISSN： 2574-8300


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  3 in total

Review 1.  Mechanisms underlying the role of ankyrin-B in cardiac and neurological health and disease.

Authors:  Nicole S York; Juan C Sanchez-Arias; Alexa C H McAdam; Joel E Rivera; Laura T Arbour; Leigh Anne Swayne
Journal:  Front Cardiovasc Med       Date:  2022-08-04

2.  Zfhx3 Transcription Factor Represses the Expression of SCN5A Gene and Decreases Sodium Current Density (INa).

Authors:  Marcos Rubio-Alarcón; Anabel Cámara-Checa; María Dago; Teresa Crespo-García; Paloma Nieto-Marín; María Marín; José Luis Merino; Jorge Toquero; Rafael Salguero-Bodes; Juan Tamargo; Jorge Cebrián; Eva Delpón; Ricardo Caballero
Journal:  Int J Mol Sci       Date:  2021-12-02       Impact factor: 5.923

Review 3.  Clinical Genetics of Inherited Arrhythmogenic Disease in the Pediatric Population.

Authors:  Estefanía Martínez-Barrios; Sergi Cesar; José Cruzalegui; Clara Hernandez; Elena Arbelo; Victoria Fiol; Josep Brugada; Ramon Brugada; Oscar Campuzano; Georgia Sarquella-Brugada
Journal:  Biomedicines       Date:  2022-01-05
  3 in total

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