Associated Papers
FHL1 mutants that cause clinically distinct human myopathies form protein aggregates and impair myoblast differentiation.
Wilding BR et al.
Journal of Cell Science, 2014
24634512 (PubMed )
Supplement: supplement_1.pdf
Reducing body myopathy and other FHL1-related muscular disorders.
Schessl J et al.
Seminars in Pediatric Neurology, 2011
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