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Congenital Short QT Syndrome

The Short QT Syndrome is a recently described new genetic disorder, characterized by abnormally short QT interval, paroxysmal atrial fibrillation and life threatening ventricular arrhythmias. This autosomal dominant syndrome can afflict infants, children, or young adults; often a remarkable family b...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Crotti, Lia, Taravelli, Erika, Girardengo, Giulia, Schwartz, Peter J
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Indian Heart Rhythm Society 2010
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2811207/
https://ncbi.nlm.nih.gov/pubmed/20126594
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