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
A case of adult-onset reducing body myopathy presenting a novel clinical feature, asymmetrical involvement of the sternocleidomastoid and trapezius muscles.
Fujii T et al.
Journal of the Neurological Sciences, 2014
Genes, proteins and complexes: the multifaceted nature of FHL family proteins in diverse tissues.
Shathasivam T et al.
Journal of Cellular and Molecular Medicine, 2010
Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy.
Gueneau L et al.
American Journal of Human Genetics, 2009
Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1.
Schessl J et al.
Brain : a Journal of Neurology, 2009
Select a paper to view details