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LMOD3 gene

Known as: LEIOMODIN 3, LMOD3 
 
National Institutes of Health

Papers overview

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2019
2019
We describe the long-term follow-up of a patient with severe nemaline myopathy due to a novel homozygous mutation in the… Expand
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Review
2017
Review
2017
Cytoskeletal structures characterized by actin filaments with uniform lengths, including the thin filaments of striated muscles… Expand
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2016
2016
BackgroundLeiomodin proteins, Lmod1, Lmod2 and Lmod3, are key regulators of the thin filament length in muscles. While Lmod1 is… Expand
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2015
2015
ABSTRACT Precise regulation of thin filament length is essential for optimal force generation during muscle contraction. The thin… Expand
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2015
2015
Update to: European Journal of Human Genetics (2012) 20; doi:10.1038/ejhg.2012.70; published online 18 April 2012 
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2015
2015
The sarcomeric tropomodulin (Tmod) isoforms Tmod1 and Tmod4 cap thin filament pointed ends and functionally interact with the… Expand
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2015
2015
ABSTRACT Nemaline myopathy (NM) is one of the most common forms of congenital myopathy, and affects either fast myofibers, slow… Expand
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Highly Cited
2014
Highly Cited
2014
Nemaline myopathy (NM) is a congenital myopathy that can result in lethal muscle dysfunction and is thought to be a disease of… Expand
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