Novel mutations in LMNA A/C gene and associated phenotypes

Mutations in the lamin A/C gene (LMNA) have been associated with several phenotypes ranging from systemic to prevalent of muscle, heart, skin, nerve etc. More recently they have been associated with dilated cardiomyopathy (DCM) and severe forms of arrhythmogenic right ventricular cardiomyopathy (ARV...

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Detalhes bibliográficos
Publicado no:Acta Myol
Main Authors: Petillo, Roberta, D'Ambrosio, Paola, Torella, Annalaura, Taglia, Antonella, Picillo, Esther, Testori, Alessandro, Ergoli, Manuela, Nigro, Gerardo, Piluso, Giulio, Nigro, Vincenzo, Politano, Luisa
Formato: Artigo
Idioma:Inglês
Publicado em: Pacini Editore SRL 2015
Assuntos:
Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4859074/
https://ncbi.nlm.nih.gov/pubmed/27199538
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