Figure 7
From: POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype
Sequence alignment of part of the spacer regions of DNA polymerase γA. The mutation sites p.R722H and p.W748S are marked with arrowheads. The sequences (and accession numbers) are: human [RefSeq:NP_001119603.1], Pan troglodytes [RefSeq:XP_523149.2], Canis familaris [RefSeq:XP_545850.2], Rattus Norwegicus [RefSeq:NP_445980.1], Mus musculus [GenBank:AAA98977.1], Gallus gallus [GenBank:AAC60018.1], Danio rerio [RefSeq:XP_001921130.1] Drosophila melanogaster [GenBank:AAF53338.1].