Andersen Syndrome: The Newest Variant of the Hereditary‐Familial Long QT Syndrome

Andersen's Syndrome is a rare disease, hereditary with autosomal dominant transmission, of the ion channels of the sarcolemmal membranes of the cardiac and skeletal muscles (channelopathy), which affects chromosome 17 of the KCNJ2 gene, responsible for encoding the outward potassium delayed rec...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Ann Noninvasive Electrocardiol
Prif Awduron: Ricardo Pérez Riera, Andrés, Ferreira, Celso, Dubner, Sérgio J., Schapachnik, Edgardo
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Blackwell Science Inc 2004
Pynciau:
Review
Edited by Shlomo Stern
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC6932481/
https://ncbi.nlm.nih.gov/pubmed/15084216
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1542-474X.2004.92552.x
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