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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study

Fig. 1

Shared haplotype of patients affected by ETFDH c.[1067G > A]. All samples listed show variable lengths of a shared haplotype on a single allele (grey) with a minimal overlapping region of 7.2 Mb, and samples P6 and P8 exhibit homozygosity (c.[1067G > A];c.[1067G > A]) for the shared haplotype (blue). The shared region includes the genes listed. These results indicate a founder for the c.[1067G > A] variant in the White SA population. Abbreviations: ETFDH electron transfer flavoprotein-ubiquinone oxidoreductase gene, GT genotype

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