Associated Papers
Unclassifiable arrhythmic cardiomyopathy associated with Emery-Dreifuss caused by a mutation in FHL1.
San Román I et al.
Clinical Genetics, 2016
Adverse clinical course and poor prognosis of hypertrophic cardiomyopathy due to mutations in FHL1.
Gallego-Delgado M et al.
International Journal of Cardiology, 2015
Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy.
Friedrich FW et al.
Human Molecular Genetics, 2012
Select a paper to view details