Very recently, mutations in the TRPM4 gene have been identified in four pedigrees as the cause of an autosomal dominant form of cardiac conduction disease. To determine the role of TRPM4 gene variations, the relative frequency of TRPM4 mutations and associated phenotypes was assessed in a cohort of
โฆ LIBER โฆ
Intracellular nucleotides and polyamines inhibit the Ca2+-activated cation channel TRPM4b
โ Scribed by Bernd Nilius; Jean Prenen; Thomas Voets; Guy Droogmans
- Publisher
- Springer
- Year
- 2004
- Tongue
- English
- Weight
- 197 KB
- Volume
- 448
- Category
- Article
- ISSN
- 0031-6768
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