Fig. 1
From: Complete APTX deletion in a patient with ataxia with oculomotor apraxia type 1
Results SNP array analysis. Indicated in the figure are the zygosity (heterozygous: yellow bars; homozygous: red bars) and Log2Ratio (reds square: deleted region based on Log2Ratio) tracks, the locations of APTX and surrounding genes on chromosome 9p21.1 (NCBI 37; UCSC hg19), and the exon numbering of APTX for our index patient (a) and the reference sample of Dr. Yoon et al. (b)