However, the fingerprint-resembling structure of the filament deposits within lmod3sa13018, as well as their location at peripheral myofiber ends, matched the sub-sarcolemmal location of filamentous fingerprint bodies described for nemaline myopathy patients [20] Thereby, lmod3-deficient zebrafish resemble aspects of the clinical symptoms of LMOD3-associated nemaline myopathy. The gene discussed is LMOD3; the disease is nemaline myopathy.