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

Author(s):
Linde, I.H.M. van der; Hiemstra, Y.L.; Bokenkamp, R.; Mil, A.M. van; Breuning, M.H. (0000-0002-8212-4319); 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.; ; Zwaag, P.A. van der; Jongbloed, J.D.H.; Bootsma, M.; Barge-Schaapveld, D.Q.C.M.
Published
2017
Publication type
Article / Letter to editor
Founder mutationCardiomyopathyCongenital heart defectBeta myosin heavy chain 7
Date issued
2017-12-31
Language
English
Is part of
Netherlands Heart Journal (2017), Vol. 25, no. 12, p. 675-681
hdl
1887/116282
doi
10.1007/s12471-017-1037-5