A Dutch MYH7 founder mutation, p.(Asn1918Lys), is associated with early onset cardiomyopathy and congenital heart defects

Linde, I.H.M. van der; Hiemstra, Y.L.; Bokenkamp, R.; Mil, A.M. van; Breuning, M.H.; Ruivenkamp, C.; ... ; Barge-Schaapveld, D.Q.C.M. (2017)

Article / Letter to editor

• Founder mutation
• Cardiomyopathy
• Congenital heart defect
• Beta myosin heavy chain 7

• All authors: Linde, I.H.M. van der; Hiemstra, Y.L.; Bokenkamp, R.; Mil, A.M. van; Breuning, M.H.; Ruivenkamp, C.; Broeke, S.W. ten; Veldkamp, R.F.; Waning, J.I. van; Slegtenhorst, M.A. van; Spaendonck-Zwarts, K.Y. van; Deprez, R.H.L.; Herkert, J.C.; L. boven; Zwaag, P.A. van der; Jongbloed, J.D.H.; Bootsma, M.; Barge-Schaapveld, D.Q.C.M.
• Date: 2017-12-31
• Journal: Netherlands Heart Journal
• Volume: 25
• Issue: 12
• Pages: 675 - 681
• DOI: doi:10.1007/s12471-017-1037-5