Llwytho...

The expression of Lamin A mutant R321X leads to endoplasmic reticulum stress with aberrant Ca(2+) handling

Mutations in the Lamin A/C gene (LMNA), which encodes A‐type nuclear Lamins, represent the most frequent genetic cause of dilated cardiomyopathy (DCM). This study is focused on a LMNA nonsense mutation (R321X) identified in several members of an Italian family that produces a truncated protein isofo...

Disgrifiad llawn

Manylion Llyfryddiaeth
Prif Awduron: Carmosino, Monica, Gerbino, Andrea, Schena, Giorgia, Procino, Giuseppe, Miglionico, Rocchina, Forleo, Cinzia, Favale, Stefano, Svelto, Maria
Fformat: Online Erthygl Texto
Iaith:English
Cyhoeddwyd: John Wiley and Sons Inc. 2016
Pynciau:
Mynediad Ar-lein:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082401/
https://www.ncbi.nlm.nih.gov/pubmed/27421120
http://dx.doi.org/10.1111/jcmm.12926