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Cardiac transplantation in an incomplete Kearns-Sayre syndrome with mitochondrial DNA deletion

  • Published:1993-01 Issue:5-6 Volume:3 Page:561-566
  • ISSN:0960-8966
  • Container-title:Neuromuscular Disorders
  • language:en
  • Short-container-title:Neuromuscular Disorders

Author:

Tranchant C.,Mousson B.,Mohr M.,Dumoulin R.,Welsch M.,Weess C.,Stepien G.,Warter J.M.

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference14 articles.

1. Mitochondrial DNA expression in mitochondrial myopathies and coordinated expression of nuclear genes involved in ATP production;Heddi;J Biol Chem,1993

2. Correlative multidisciplinary approach to the study of mitochondrial encephalomyopathies;Karpati;Rev Neurol (Paris),1991

3. Deletions of mitochondrial DNA in patients with mitochondrial myopathies;Holt;Nature,1988

4. Kearns-Sayre syndrome with muscle mitochondrial DNA deletion;Lestienne;Lancet,1988

5. Deletions of mitochondrial DNA in Kearns-Sayre syndrome;Zeviani;Neurology,1988

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