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...

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Bibliografische gegevens
Gepubliceerd in:Nucleus
Hoofdauteurs: Tu, Yiping, Sánchez-Iglesias, Sofía, Araújo-Vilar, David, Fong, Loren G., Young, Stephen G.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Taylor & Francis 2016
Onderwerpen:
Research Paper
Online toegang: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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