Mitochondrial myopathy and ophthalmoplegia in a sporadic patient with the G12315A mutation in mitochondrial DNA.
- 1 November 2002
- journal article
- case report
- Published by Elsevier BV in Neuromuscular Disorders
- Vol. 12 (9), 865-868
- https://doi.org/10.1016/s0960-8966(02)00072-x