Severe myopathy in mice lacking the MEF2/SRF-dependent gene leiomodin-3-Reference-Cited by-同舟云学术

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Severe myopathy in mice lacking the MEF2/SRF-dependent gene leiomodin-3

Published:2015-03-16 Issue:4 Volume:125 Page:1569-1578
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Cenik Bercin K.,Garg Ankit,McAnally John R.,Shelton John M.,Richardson James A.,Bassel-Duby Rhonda,Olson Eric N.,Liu Ning

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference55 articles.

1. Clinical course correlates poorly with muscle pathology in nemaline myopathy

2. Congenital myopathies

3. Recent advances in nemaline myopathy

4. North KN, Ryan MM. Nemaline Myopathy. GeneReviews. Seattle, Washington, USA: University of Washington; 2002.

5. Skeletal muscle α-actin diseases (actinopathies): pathology and mechanisms

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1. A nemaline myopathy–linked mutation inhibits the actin-regulatory functions of tropomodulin and leiomodin;Proceedings of the National Academy of Sciences;2023-11-13

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3. Case report: Homozygous variants of NEB and KLHL40 in two Arab patients with nemaline myopathy;Frontiers in Genetics;2023-03-21

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