Laminopathies
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Laminopathy
Laminopathies are rare genetic disorders. They are caused by mutations in the LMNA gene that encodes two proteins: lamin A and C, which are essential for maintaining the structure and function of the cell nucleus. This genetic disorder causes several diseases, including lamin A/C cardiomyopathy, also known as cardiolaminopathy, which mainly affects the heart and…
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