Abstract
Mitochondrial genetic modifying factors have been suspected in several autosomally inherited diseases. The congenital variant of myotonic dystrophy, in which there is a striking maternal inheritance pattern, is a likely candidate disease. To investigate this possibility, we sequenced completely the mitochondrial genome in 2 patients with congential myotonic dystrophy. Comparison of the two sequences with control data failed to reveal a specific nucleotide variant or length variant in this disease. We conclude that a mitochondrial genetic modifying factor is not present in congenital myotonic dystrophy.
| Original language | English |
|---|---|
| Pages (from-to) | 724-727 |
| Number of pages | 4 |
| Journal | Annals of Neurology |
| Volume | 30 |
| Issue number | 5 |
| DOIs | |
| Publication status | Published - Nov 1991 |
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