Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin (DES) Mutation p.Y122H Leading to a Severe Filament Assembly Defect

por Brodehl, Andreas, Pour Hakimi, Seyed Ahmad, Stanasiuk, Caroline, Ratnavadivel, Sandra, Hendig, Doris, Gaertner, Anna, Gerull, Brenda, Gummert, Jan, Paluszkiewicz, Lech, Milting, Hendrik
Publicado 2019