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
Verfasser: | |
---|---|
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-26677088 |
Datenquelle: | BASE; Originalkatalog |
Powered By: | BASE |
Link(s) : | http://repub.eur.nl/pub/103326 |