Clinical Manifestation of Nebulin-Associated Nemaline Myopathy
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DOI: 10.1212/nxg.0000000000200056
Abstract: Background and Objectives Nemaline myopathy (NM) is a genetically heterogeneous inherited myopathy related with at least 12 genes, whereas pathogenic variants in NEB gene are the most common genetic cause. The clinical spectrum of NM… read more here.
Keywords: age; patients neb; nemaline myopathy; support ... See more keywords