Associated Papers
Evidence of mild founder LMOD3 mutations causing nemaline myopathy 10 in Germany and Austria.
Schatz UA et al.
Neurology, 2018
Neonatal fractures as a presenting feature of LMOD3-associated congenital myopathy.
Abbott M et al.
American Journal of Medical Genetics. Part A, 2017
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy.
Yuen M et al.
The Journal of Clinical Investigation, 2015
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy.
Yuen M et al.
The Journal of Clinical Investigation, 2014
Select a paper to view details