Functional Characterization of Rare Variants in the SHOX2 Gene Identified in Sinus Node Dysfunction and Atrial Fibrillation

Sinus node dysfunction (SND) and atrial fibrillation (AF) often coexist; however, the molecular mechanisms linking both conditions remain elusive. Mutations in the homeobox-containing SHOX2 gene have been recently associated with early-onset and familial AF. Shox2 is a key regulator of sinus node de...

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Detalles Bibliográficos
Autores principales: Hoffmann, Sandra, Paone, Christoph, Sumer, Simon A., Diebold, Sabrina, Weiss, Birgit, Roeth, Ralph, Clauss, Sebastian, Klier, Ina, Kääb, Stefan, Schulz, Andreas, Wild, Philipp S., Ghrib, Adil, Zeller, Tanja, Schnabel, Renate B., Just, Steffen, Rappold, Gudrun A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637028/
https://www.ncbi.nlm.nih.gov/pubmed/31354791
http://dx.doi.org/10.3389/fgene.2019.00648

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637028/
https://www.ncbi.nlm.nih.gov/pubmed/31354791
http://dx.doi.org/10.3389/fgene.2019.00648

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