Associated Papers
Clinical and genetic analysis of a family with myopathy caused by an FHL1 gene variant.
Zhang S et al.
Bmj Neurology Open, 2025
FHL1-mutated reducing body myopathy.
Lim KY et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology, 2020
Unclassifiable arrhythmic cardiomyopathy associated with Emery-Dreifuss caused by a mutation in FHL1.
San Román I et al.
Clinical Genetics, 2016
FHL1 mutants that cause clinically distinct human myopathies form protein aggregates and impair myoblast differentiation.
Wilding BR et al.
Journal of Cell Science, 2014
Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy.
Friedrich FW et al.
Human Molecular Genetics, 2012
Identification of FHL1 as a regulator of skeletal muscle mass: implications for human myopathy.
Cowling BS et al.
The Journal of Cell Biology, 2008
Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy.
Schessl J et al.
The Journal of Clinical Investigation, 2008
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