Unfortunately, the published article has errors in Table 1. In second case with MFN2 mutation the deleted nucleotides are c.298_299GC and they are replaced by TT, thus resulting into a p.Ala100Phe change. Subcloning was used to discriminate delins in cis against two substitutions in trans. In the fourth case with GJB1 mutation results were originally annotated as c.472C>G causing p.Pro158Ala (“c.534C>G” was likely a typo.). The correct Table 1 is given in the following page. We thank a reader (Dr Andrew Phillips) who signaled us these mistakes.
- Neurology (clinical)