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A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding gene

  • Published:1995-09 Issue:5 Volume:5 Page:391-398
  • ISSN:0960-8966
  • Container-title:Neuromuscular Disorders
  • language:en
  • Short-container-title:Neuromuscular Disorders

Author:

Manfredi G.,Schon E.A.,Moraes C.T.,Bonilla E.,Berry G.T.,Sladky J.T.,Dimauro S.

Publisher

Elsevier BV

Subject

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

Reference31 articles.

1. Sequence and organization of the human mitochondrial genome;Anderson;Nature,1981

2. Mitochondrial encephalomyopathies: clinical and molecular analysis;Wallace;J Bioenerg Biomembr,1994

3. Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutation;Shoffner;Cell,1990

4. A new mtDNA mutation in the tRNAlys gene associated with myoclinic epilepsy and ragged-red fibers (MERRF);Silvestri;Am J Hum Genet,1992

5. A mutation in the tRnALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies;Goto;Nature,1990
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