Molecular autopsy and family screening in a young case of sudden cardiac death reveals an unusually severe case of FHL1 releated hypertrophic cardiomyopathy
Gaertner-Rommel A, Tiesmeier J, Jakob T, Strickmann B, Veit G, Bachmann-Mennenga B, Paluszkiewicz L, Klingel K, Schulz U, Laser T, Karger B, Pfeiffer H, Milting H
Research article (journal) | Peer reviewed
Details about the publication
Volume: 7
Status: online first
Release year: 2019
Language in which the publication is written: English