Molecular Diagnosis of Friedreich Ataxia Using Analysis of GAA Repeats and FXN Gene Exons in Population from Western India
Figure 3
Shows BioEdit analysis of exon 2 of the FXN gene in normal individual, FRDA negative patient and one uninformative patient, which showed mutation at A226C and Ins246T. The sites of mutation in exon 2 have been highlighted by boxes.
