LMOD3: the "missing link" in nemaline myopathy?

Oncotarget. 2015 Sep 29;6(29):26548-9. doi: 10.18632/oncotarget.5267.

Authors

Sarah Sandaradura¹, Kathryn N North²

Affiliations

¹ Institute for Neuroscience and Muscle Research, The Children's Hospital at Westmead and Discipline of Paediatrics and Child Health, University of Sydney, New South Wales, Australia.
² Murdoch Children's Research Institute, The Royal Children's Hospital and Department of Paediatrics, University of Melbourne, Victoria, Australia.

No abstract available

Keywords: congenital myopathy; genetics; muscle; nemaline myopathy.

Publication types

Editorial

MeSH terms

Actins / biosynthesis
Animals
Cytoskeleton / metabolism
Genes, Recessive
Humans
Mice
Mice, Knockout
Microfilament Proteins / genetics
Microfilament Proteins / metabolism
Muscle Hypotonia
Muscle Proteins / genetics
Muscle Proteins / metabolism*
Muscle, Skeletal / metabolism
Muscle, Skeletal / pathology
Mutation
Myopathies, Nemaline / pathology*
Phenotype
Protein Binding
Xenopus

Substances

Actins
LMOD3 protein, human
Microfilament Proteins
Muscle Proteins
leiomodin-3 protein, mouse