Novel CALM3 mutations in pediatric long QT syndrome patients support a CALM3-specific calmodulinopathy
oleh: Marie-A. Chaix, MD, MSc, Tamara T. Koopmann, PhD, Philippe Goyette, PhD, Azadeh Alikashani, MSc, Frédéric Latour, MSc, Meena Fatah, HBSc, Robert M. Hamilton, MD, John D. Rioux, PhD
| Format: | Article |
|---|---|
| Diterbitkan: | Elsevier 2016-05-01 |
Deskripsi
Subjek
Long QT syndrome; Calmodulin; CALM3; Whole exome sequencing