Cargando…
Low and High Expressing Alleles of the LMNA Gene: Implications for Laminopathy Disease Development
Today, there are at least a dozen different genetic disorders caused by mutations within the LMNA gene, and collectively, they are named laminopathies. Interestingly, the same mutation can cause phenotypes with different severities or even different disorders and might, in some cases, be asymptomati...
Autores principales: | Rodríguez, Sofía, Eriksson, Maria |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3183053/ https://www.ncbi.nlm.nih.gov/pubmed/21980471 http://dx.doi.org/10.1371/journal.pone.0025472 |
Ejemplares similares
-
A truncated lamin A in the Lmna(−/−) mouse line: Implications for the understanding of laminopathies
por: Jahn, Daniel, et al.
Publicado: (2012) -
Challenging the “chromatin hypothesis” of cardiac laminopathies with LMNA mutant iPS cells
por: Mozzetta, Chiara, et al.
Publicado: (2019) -
Disheveled Hair and Ear (Dhe), a Spontaneous Mouse Lmna Mutation Modeling Human Laminopathies
por: Odgren, Paul R., et al.
Publicado: (2010) -
Heterozygous LMNA mutation-carrying iPSC lines from three cardiac laminopathy patients
por: Cho, Sangkyun, et al.
Publicado: (2022) -
A subtype of laminopathies: Generalized lipodystrophy‐associated progeroid syndrome caused by LMNA gene c.29C>T mutation
por: Huang, Shipeng, et al.
Publicado: (2023)