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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Acta Myol
Päätekijät: Petillo, Roberta, D'Ambrosio, Paola, Torella, Annalaura, Taglia, Antonella, Picillo, Esther, Testori, Alessandro, Ergoli, Manuela, Nigro, Gerardo, Piluso, Giulio, Nigro, Vincenzo, Politano, Luisa
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Pacini Editore SRL 2015
Aiheet:
Original Articles
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4859074/
https://ncbi.nlm.nih.gov/pubmed/27199538
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