Nemaline myopathy 3

Known as: NEM3, Nemaline myopathy caused by mutation in the alpha-actin gene 
 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
OBJECTIVE Nemaline myopathy (NM) is one of the most common congenital nondystrophic myopathies and is characterized by muscle… (More)
  • table 1
  • figure 1
  • figure 2
  • table 2
  • figure 3
Is this relevant?
2015
2015
Update to: European Journal of Human Genetics (2012) 20; doi:10.1038/ejhg.2012.70; published online 18 April 2012 
Is this relevant?