A G613A missense in the Hutchinson’s progeria lamin A/C gene causes a lone, autosomal dominant atrioventricular block

BACKGROUND: LMNA/C mutations have been linked to the premature aging syndrome Hutchinson’s progeria, dilated cardiomyopathy 1A, skeletal myopathies (such as the autosomal dominant variant of Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy), Charcot-Marie-Tooth disorder type 2B1,...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Immun Ageing
Main Authors: Villa, Francesco, Maciąg, Anna, Spinelli, Chiara C, Ferrario, Anna, Carrizzo, Albino, Parisi, Attilio, Torella, Annalaura, Montenero, Chiara, Condorelli, Gianluigi, Vecchione, Carmine, Nigro, Vincenzo, Montenero, Annibale S, Puca, Annibale A
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2014
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4251685/
https://ncbi.nlm.nih.gov/pubmed/25469153
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12979-014-0019-3
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados