Discordant Gene Expression Signatures and Related Phenotypic Differences in Lamin A- and A/C-Related Hutchinson-Gilford Progeria Syndrome (HGPS)

Hutchinson-Gilford progeria syndrome (HGPS) is a genetic disorder displaying features reminiscent of premature senescence caused by germline mutations in the LMNA gene encoding lamin A and C, essential components of the nuclear lamina. By studying a family with homozygous LMNA mutation (K542N), we s...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Plasilova, Martina, Chattopadhyay, Chandon, Ghosh, Apurba, Wenzel, Friedel, Demougin, Philippe, Noppen, Christoph, Schaub, Nathalie, Szinnai, Gabor, Terracciano, Luigi, Heinimann, Karl
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2011
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3124505/
https://ncbi.nlm.nih.gov/pubmed/21738662
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0021433
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados