PathologyCardiovascular ResearchPeer-reviewed
The p.H222P lamin A/C mutation induces heart failure via impaired mitochondrial calcium uptake in human cardiac laminopathy
Magali Seguret, Charlène Jouve, Andrea Ruiz‐Velasco…·Jean‐Sébastien Hulot
This study investigates how the LMNA p.H222P mutation causes heart failure by impairing mitochondrial calcium uptake in human cardiac cells.
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