/
Am J Med Genet C Semin Med Genet
Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7
- A.M. Vermeer
- K. van Engelen
- A.V. Postma
- M.J. Baars
- I. Christiaans
- S. De Haij
- S. Klaassen
- B.J. Mulder
- B. Keavney