Unraveling <i>LMNA</i> Mutations in Metabolic Syndrome: Cellular Phenotype and Clinical Pitfalls
This study details the clinical and cellular phenotypes associated with two missense heterozygous mutations in <i>LMNA</i>, c.1745G>T p.(Arg582Leu), and c.1892G>A p.(Gly631Asp), in two patients with early onset of diabetes mellitus, hypertriglyceridemia and non-alcoholic fa...
Main Authors: | , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2020-01-01
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Series: | Cells |
Subjects: | |
Online Access: | https://www.mdpi.com/2073-4409/9/2/310 |