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A common mitochondrial DNA variant is associated with susceptibility to idiopathic dilated cardiomyopathy in two different populations.

A common mitochondrial DNA variant is associated with susceptibility to idiopathic dilated cardiomyopathy in two different populations.

Manylion Llyfryddiaeth
Prif Awduron: Khogali, S, Mayosi, B, Beattie, J, McKenna, W, Watkins, H, Poulton, J
Fformat: Journal article
Cyhoeddwyd: 2000
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Eitemau Tebyg

  • A common mitochondrial DNA variant is associated with idiopathic dilated cardiomyopathy in two different populations
    gan: Khogali, S, et al.
    Cyhoeddwyd: (2000)
  • A common mitochondrial DNA variant associated with susceptibility to dilated cardiomyopathy in two different populations.
    gan: Khogali, S, et al.
    Cyhoeddwyd: (2001)
  • Association of a common mitochondrial DNA D-loop variant with idiopathic dilated cardiomyopathy in two different populations
    gan: Khogali, S, et al.
    Cyhoeddwyd: (2000)
  • Identification of a novel mitochondrial DNA mutation in the ND1 gene in 2 patients with hypertrophic cardiomyopathy with restrictive physiology
    gan: Khogali, S, et al.
    Cyhoeddwyd: (2001)
  • Identification of a novel mitochondrial NADH dehydrogenase I (MTND1) gene mutation in two patients with hypertrophic cardiomyopathy
    gan: Khogali, S, et al.
    Cyhoeddwyd: (2001)

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