Lamin Mutations Cause Increased YAP Nuclear Entry in Muscle Stem Cells
Mutations in the <i>LMNA</i> gene, encoding the nuclear envelope A-type lamins, are responsible for muscular dystrophies, the most severe form being the <i>LMNA</i>-related congenital muscular dystrophy (L-CMD), with severe defects in myonucleus integrity. We previously repor...
Main Authors: | , , , , , , |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2020-03-01
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Series: | Cells |
Subjects: | |
Online Access: | https://www.mdpi.com/2073-4409/9/4/816 |