Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth
Laminopathies are a clinically heterogeneous group of disorders caused by mutations in the <i>LMNA</i> gene, which encodes the nuclear envelope proteins lamins A and C. The most frequent diseases associated with <i>LMNA</i> mutations are characterized by skeletal and cardiac...
Main Authors: | , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2020-12-01
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Series: | International Journal of Molecular Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/1422-0067/22/1/306 |