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Mitochondrial disease associated with the T8993G mutation of the mitochondrial ATPase 6 gene: a clinical, biochemical, and molecular study in six families
  1. Dr Massimo Zeviani, Division of Biochemistry and Genetics, Istituto Nazionale Neurologico “Carlo Besta”, Via Celoria 11, Milano 20133, Italy.
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Citation

Uziel G, Moroni I, Lamantea E, et al
Mitochondrial disease associated with the T8993G mutation of the mitochondrial ATPase 6 gene: a clinical, biochemical, and molecular study in six families

Publication history

  • Received November 11, 1996
  • Revised February 12, 1997
  • Accepted February 14, 1997
  • First published July 1, 1997.
Online issue publication 
April 13, 2016

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