Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations

Aims: Mutations in the lamin A/C gene (LMNA) have been reported to be involved in dilated cardiomyopathy (DCM) associated with conduction system disease and/or skeletal myopathy. The aim of this study was to perform a mutational analysis of LMNA in a large white population of patients affected by di...

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Autors principals: Sebillon, P, Bouchier, C, Bidot, L, Bonne, G, Ahamed, K, Charron, P, Drouin-Garraud, V, Millaire, A, Desrumeaux, G, Benaiche, A, Charniot, J, Schwartz, K, Villard, E, Komajda, M
Format: Artigo
Idioma:Inglês
Publicat: BMJ Group 2003
Matèries:
Original Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1735561/
https://ncbi.nlm.nih.gov/pubmed/12920062
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.40.8.560
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