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Volume 2 Issue 1 Volume 1 Issue 1

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2019-02-22 Review Article

The role of genetic mutations in genes LMNA, PPARG, PLIN1, AKT2, CIDEC in Kobberling–Dunnigan Syndrome

Kobberling-Dunnigan syndrome, also known as partial familial lipodystrophy, is a rare genetic disorder characterized by abnormal distribution of adipose tissues. Many people with Kobberling-
Dunnigan syndrome develop insulin resistance, a condition in which body tissues cannot adequate...

Read Full Article HTML DOI: 10.29328/journal.jgmgt.1001004 Citation