Fig. 2From: A 9-year-old Korean girl with Fontaine progeroid syndrome: a case report with further phenotypical delineation and description of clinical course during long-term follow-upSanger-sequencing chromatogram of our patient. Partial sequencing of the cloning allele of SLC25A24 showed the presence of a heterozygous missense mutation, NM_013386:c.650G > A, p.[Arg217His], in exon 5Back to article page