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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
- Dr Massimo Zeviani, Division of Biochemistry and Genetics, Istituto Nazionale Neurologico “Carlo Besta”, Via Celoria 11, Milano 20133, Italy.
Citation
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
July 01, 1997
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Journal of Neurology, Neurosurgery, and Psychiatry