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Fig. 2 | BMC Medical Genomics

Fig. 2

From: Novel intragenic deletion within the FXN gene in a patient with typical phenotype of Friedreich ataxia: may be more prevalent than we think?

Fig. 2

Deletion/duplication analysis of FXN gene and summary of intragenic deletions reported to date. (A) MLPA analysis with the kit P316-B4 showed a deletion of FXN exons 1 and 2 in the mother (II-4) and the proband’s (III-2) samples. The deleted probes are highlighted in red. (B) Summary of FXN gene deletions in the literature and this report

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BMC Medical Genomics

ISSN: 1755-8794

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