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
FHL1 mutants that cause clinically distinct human myopathies form protein aggregates and impair myoblast differentiation.
Wilding BR et al.
Journal of Cell Science, 2014
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