TY  - GEN 
AU  - Gerhardt, T.
AU  - Monserrat Iglesias, Lorenzo
AU  - Landmesser, U.
AU  - Poller, W.
PY  - 2022
SN  - 2514-2119
UR  - http://hdl.handle.net/20.500.11940/20678
AB  - Background: Restrictive cardiomyopathy is rare and heterogeneous in origin, clinical manifestation, and prognosis. Familial forms have, amongst others, been associated with mutations in the TNNI3 gene. We present a case of familial restrictive...
LA  - eng
TI  - A novel Troponin I mutation associated with severe restrictive cardiomyopathy - A case report of a 27-year-old woman with fatigue
DO  - 10.1093/ehjcr/ytac053
KW  - AS Coruña
KW  - CHUAC
KW  - INIBIC
VL  - 6
ER  -