Articles with "kbtbd13 related" as a keyword



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NEM6, KBTBD13-Related Congenital Myopathy: Myopathological Analysis in 18 Dutch Patients Reveals Ring Rods Fibers, Cores, Nuclear Clumps, and Granulo-Filamentous Protein Material.

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Published in 2021 at "Journal of neuropathology and experimental neurology"

DOI: 10.1093/jnen/nlab012

Abstract: Nemaline myopathy type 6 (NEM6), KBTBD13-related congenital myopathy is caused by mutated KBTBD13 protein that interacts improperly with thin filaments/actin, provoking impaired muscle-relaxation kinetics. We describe muscle morphology in 18 Dutch NEM6 patients and correlate… read more here.

Keywords: kbtbd13 related; congenital myopathy; microscopy; ring rods ... See more keywords