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LMNA missense mutations causing familial partial lipodystrophy do not lead to an accumulation of prelamin A
A variety of missense mutations in LMNA (the gene for lamin C and prelamin A) cause familial partial lipodystrophy (FPLD), a disease associated with reduced adipose tissue, particularly in the limbs. Several studies have reported that fibroblasts from FPLD subjects have an accumulation of prelamin A...
Tallennettuna:
| Julkaisussa: | Nucleus |
|---|---|
| Päätekijät: | , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Taylor & Francis
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5120598/ https://ncbi.nlm.nih.gov/pubmed/27841971 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19491034.2016.1242542 |
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