Caricamento...
Morphological analysis of 13 LMNA variants identified in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy
BACKGROUND: Mutations in the LMNA gene, encoding lamins A/C, represent a significant cause of dilated cardiomyopathy (DCM). We recently identified 18 protein-altering LMNA variants in a cohort of 324 unrelated patients with DCM. However, at least one family member with DCM in each of six pedigrees l...
Salvato in:
| Autori principali: | , , , , |
|---|---|
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2009
|
| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2908895/ https://ncbi.nlm.nih.gov/pubmed/20160190 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGENETICS.109.905422 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|