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© Research
Publication : Journal of medical genetics

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

Scientific Fields
Diseases
Organisms
Applications
Technique

Published in Journal of medical genetics - 01 Aug 2003

Sébillon P, Bouchier C, Bidot LD, Bonne G, Ahamed K, Charron P, Drouin-Garraud V, Millaire A, Desrumeaux G, Benaïche A, Charniot JC, Schwartz K, Villard E, Komajda M

Link to Pubmed [PMID] – 12920062

J. Med. Genet. 2003 Aug;40(8):560-7

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 dilated cardiomyopathy with or without associated symptoms.

http://www.ncbi.nlm.nih.gov/pubmed/12920062