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Fig. 1 | Cellular & Molecular Biology Letters

Fig. 1

From: Identification of a novel deletion in the MMAA gene in two Iranian siblings with vitamin B12-responsive methylmalonic acidemia

Fig. 1

Family pedigree and DNA sequence chromatograms of family members (a) Family pedigree and mutation analysis for exon 4 of MMAA (b) A DNA sequence chromatogram of the family members (B1) DNA sequence chromatogram of the affected daughter (4 years old) with the homozygous c.674delA mutation (B2) DNA sequence chromatogram of the affected son (1.5 years old) with the homozygous c.674delA mutation (B3) DNA sequence chromatogram of the father with the heterozygous c.674delA mutation (B4) DNA sequence chromatogram of the mother with the heterozygous c.674delA mutation (B5) DNA sequence chromatogram of the unaffected son with the heterozygous c.674delA mutation

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