Transient receptor potential channelopathies
- PMID: 20127491
- DOI: 10.1007/s00424-010-0788-2
Transient receptor potential channelopathies
Abstract
In the past years, several hereditary diseases caused by defects in transient receptor potential channels (TRP) genes have been described. This review summarizes our current knowledge about TRP channelopathies and their possible pathomechanisms. Based on available genetic indications, we will also describe several putative pathological conditions in which (mal)function of TRP channels could be anticipated.
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