Mutation Load of Multiple Ion Channel Gene Mutations in Brugada Syndrome

Publisher： Karger

E-ISSN： 1421-9751|137|4|256-260

ISSN： 0008-6312

Source： Cardiology, Vol.137, Iss.4, 2017-05, pp. : 256-260

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Gain‐of‐Function KCNH2 Mutations in Patients with Brugada Syndrome

By  

JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, Vol. 25, Iss. 5, 2014-05 ,pp. : 522-530

John Wiley & Sons Inc

Access to resources Recommend Favorite

Two novel Brugada syndrome-associated mutations increase KV4.3 membrane expression and function

By          

International Journal of Molecular Medicine, Vol. 36, Iss. 1, 2015-01 ,pp. : 309-315

Spandidos Publications

Access to resources Recommend Favorite

Genetic biomarkers in Brugada syndrome

By Li Anthony   Saba Magdi M   Behr Elijah R  

Biomarkers in Medicine, Vol. 7, Iss. 4, 2013-08 ,pp. : 535-546

Future Medicine

Access to resources Recommend Favorite

Brooke‐Spiegler syndrome presenting multiple concurrent cutaneous and parotid gland neoplasms: Cytologic findings on fine‐needle sample and description of a novel mutation of the CYLD gene

By  

DIAGNOSTIC CYTOPATHOLOGY, Vol. 43, Iss. 8, 2015-08 ,pp. : 654-658

John Wiley & Sons Inc

Access to resources Recommend Favorite

Brugada syndrome unmasked by lithium therapy

By Schernthaner Christiana   Strohmer Bernhard  

Wiener klinische Wochenschrift, Vol. 119, Iss. 9-10, 2007-06 ,pp. : 282-282

Springer Publishing Company

Access to resources Recommend Favorite