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...
المؤلفون الرئيسيون: | Khogali, S, Mayosi, B, Beattie, J, McKenna, W, Watkins, H, Poulton, J |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
2000
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مواد مشابهة
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A common mitochondrial DNA variant is associated with susceptibility to idiopathic dilated cardiomyopathy in two different populations.
حسب: Khogali, S, وآخرون
منشور في: (2000) -
Association of a common mitochondrial DNA D-loop variant with idiopathic dilated cardiomyopathy in two different populations
حسب: Khogali, S, وآخرون
منشور في: (2000) -
A common mitochondrial DNA variant associated with susceptibility to dilated cardiomyopathy in two different populations.
حسب: Khogali, S, وآخرون
منشور في: (2001) -
Identification of a novel mitochondrial DNA mutation in the ND1 gene in 2 patients with hypertrophic cardiomyopathy with restrictive physiology
حسب: Khogali, S, وآخرون
منشور في: (2001) -
Identification of a novel mitochondrial NADH dehydrogenase I (MTND1) gene mutation in two patients with hypertrophic cardiomyopathy
حسب: Khogali, S, وآخرون
منشور في: (2001)