Figure 3
From: A MELAS syndrome family harboring two mutations in mitochondrial genome
Haplogroup classification based on complete mtDNA genome sequence in the MT48 patients. The mtDNA mutations identified in the patient suggested M7c2 haplogroup-specific. Numbers refer to substitutions at nucleotide positions with respect to the revised Cambridge reference sequence (rCRC). The suffixes indicate transversions, and underlines indicate recurrent mutations. Others indicate transitions. Open boxes represent mutations observed in the patients implicating the M7c2 haplogroup, and grayed box represents the private mutations specific for MT48 family.
