Gain-of-function mutations in TRPM4 cause autosomal dominant isolated cardiac conduction disease.
Abstract
Isolated cardiac conduction block is a relatively common condition in young and elderly populations. Genetic predisposing factors have long been suspected because of numerous familial case reports. Deciphering genetic predisposing factors of conduction blocks may give a hint at stratifying conduction block carriers in a more efficient way.
Bibliographical data
| Original language | German |
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| Article number | 4 |
| ISSN | 1942-325X |
| Publication status | Published - 2010 |
| pubmed | 20562447 |
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