Acute peripheral neuropathy, rhabdomyolysis, and severe lactic acidosis associated with 3243 A to G mitochondrial DNA mutation.
- 1 December 1994
- journal article
- Published by BMJ in Journal of Neurology, Neurosurgery & Psychiatry
- Vol. 57 (12) , 1545-1546
- https://doi.org/10.1136/jnnp.57.12.1545-a
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)Biochemical and Biophysical Research Communications, 1991
- Pathological Findings of the Sural Nerve in Mitochondrial EncephalomyopathyPsychiatry and Clinical Neurosciences, 1988
- Peripheral neuropathy associated with mitochondrial myopathyAnnals of Neurology, 1986
- Neuropathy and mitochondrial myopathyAnnals of Neurology, 1980
- Lactic acidemia, mitochondrial myopathy, and basal ganglia calcificationNeurology, 1979