Homozygous and Heterozygous Nuclear Lamin A p.R582C Mutation: Different Lipodystrophic Phenotypes in the Same Kindred.

Front Endocrinol (Lausanne) · 2018 · PMC6110164 · PMID 30177912

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did not reach statistical significanceno p-value reported

The frequency of diabetes, hypertension, dyslipidemia, and hepatic steatosis tended to be higher in the homozygous group but did not reach statistical significance.

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