A common mitochondrial DNA variant is associated with idiopathic dilated cardiomyopathy in two different populations
Dilated Cardiomyopathy (DCM) is a devastating disease. It is a recognised manifestation of mitochondrial disease and in some cases the only clinical abnormality. Although specific mitochondrial DNA(mtDNA) mutations in tRNAleu/lle have been identified in mitochondrial disease associated with DCM, it...
Autores principales: | Khogali, S, Mayosi, B, Beattie, J, McKenna, W, Watkins, H, Poulton, J |
---|---|
Formato: | Journal article |
Lenguaje: | English |
Publicado: |
2000
|
Ejemplares similares
-
A common mitochondrial DNA variant is associated with susceptibility to idiopathic dilated cardiomyopathy in two different populations.
por: Khogali, S, et al.
Publicado: (2000) -
Association of a common mitochondrial DNA D-loop variant with idiopathic dilated cardiomyopathy in two different populations
por: Khogali, S, et al.
Publicado: (2000) -
A common mitochondrial DNA variant associated with susceptibility to dilated cardiomyopathy in two different populations.
por: Khogali, S, et al.
Publicado: (2001) -
Identification of a novel mitochondrial DNA mutation in the ND1 gene in 2 patients with hypertrophic cardiomyopathy with restrictive physiology
por: Khogali, S, et al.
Publicado: (2001) -
Identification of a novel mitochondrial NADH dehydrogenase I (MTND1) gene mutation in two patients with hypertrophic cardiomyopathy
por: Khogali, S, et al.
Publicado: (2001)