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