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

Background Mutations in the myosin heavy chain 7 (MYH7) gene commonly cause cardiomyopathy but are less frequently associated with congenital heart defects. Methods In thi

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Verfasser: van der Linde, I.H.M. (I. H.M.)
Hiemstra, Y.L. (Y. L.)
Bökenkamp, A. (Arend)
Mil, A.M. (Anneke) van
Breuning, M.H. (Martijn)
Ruivenkamp, C.A. (Claudia)
Ten Broeke, S.W. (Sanne W.)
Veldkamp, R.F. (Rolf)
Waning, J. (Jaap) van
Slegtenhorst, M.A. (Marjon) van
Spaendonck-Zwarts, K.Y. (Karin) van
Lekanne Deprez, R.H.
Herkert, J.C. (Johanna)
Boven, L.G. (Ludolf)
Zwaag, P.A. (Paul) van der
Jongbloed, J.D.H. (Jan)
Bootsma, M. (Marianne)
Barge-Schaapveld, D.Q.C.M. (Daniela)
Dokumenttyp: Artikel
Erscheinungsdatum: 2017
Schlagwörter: Beta myosin heavy chain 7 / Cardiomyopathy / Congenital heart defect / Founder mutation
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-29035073
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : http://repub.eur.nl/pub/103326