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A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene. [electronic resource] by
- Priori, Silvia G
- Pandit, Sandeep V
- Rivolta, Ilaria
- Berenfeld, Omer
- Ronchetti, Elena
- Dhamoon, Amit
- Napolitano, Carlo
- Anumonwo, Justus
- di Barletta, Marina Raffaele
- Gudapakkam, Smitha
- Bosi, Giuliano
- Stramba-Badiale, Marco
- Jalife, José
Producer: 20051011
In:
Circulation research vol. 96
Availability: No items available.
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