Congenital short QT syndrome: landmarks of the newest arrhythmogenic cardiac channelopathy
Congenital short QT syndrome: landmarks of the newest arrhythmogenic cardiac channelopathy
About this item
Full title
Author / Creator
Publisher
Poland: Wydawnictwo Via Medica
Journal title
Language
English
Formats
Publication information
Publisher
Poland: Wydawnictwo Via Medica
Subjects
More information
Scope and Contents
Contents
Congenital or familial short QT syndrome is a genetically heterogeneous cardiac channelopathy without structural heart disease that has a dominant autosomal or sporadic pattern of transmission affecting the electric system of the heart. Patients present clinically with a spectrum of signs and symptoms including irregular palpitations due to episode...
Alternative Titles
Full title
Congenital short QT syndrome: landmarks of the newest arrhythmogenic cardiac channelopathy
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_1464908162
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1464908162
Other Identifiers
ISSN
1897-5593
E-ISSN
1897-5593,1898-018X
DOI
10.5603/CJ.a2013.0052
