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Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicity.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 3152, doi. 10.1093/hmg/ddt172
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- Publication type:
- Article
DelK32-lamin A/C has abnormal location and induces incomplete tissue maturation and severe metabolic defects leading to premature death.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1037, doi. 10.1093/hmg/ddr534
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- Publication type:
- Article