No abstract available
MeSH terms
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Aging / genetics*
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Cardiomyopathy, Dilated / genetics
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Cardiomyopathy, Dilated / therapy
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DNA Damage
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Female
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Humans
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Lamin Type A / genetics*
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Lipodystrophy / etiology
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Lipodystrophy / genetics*
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Lipodystrophy / therapy
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Models, Biological
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Mutation, Missense
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Primary Ovarian Insufficiency / genetics
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Primary Ovarian Insufficiency / therapy
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Syndrome
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Werner Syndrome / etiology
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Werner Syndrome / genetics*
Substances
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LMNA protein, human
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Lamin Type A