Showing results 1 to 2 of 2
Title | Author(s) | Issue Date | |
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Clinical spectrum and genetic variations of LMNA-related muscular dystrophies in a large cohort of Chinese patients Journal:Journal of Medical Genetics | 2020 | ||
Cytoplasmic body pathology in severe ACTA1-related myopathy in the absence of typical nemaline rod histology Proceeding/Conference:Neuromuscular Disorders | 2015 |