Article
Genotype and phenotype analyses in 136 patients with single large-scale mitochondrial DNA deletions.
Journal of human genetics - 1 Jan 2008
Yamashita Shintaro, Nishino Ichizo, Nonaka Ikuya, Goto Yu-Ichi
Abstract excerpt
We examined 136 patients with mitochondrial DNA (mtDNA) deletion. Clinical diagnoses included chronic progressive external ophthalmoplegia (94 patients); Kearns-Sayre syndrome (KSS; 33 patients); Pearson's marrow-pancreas syndrome (six patients); and Leigh syndrome, Reye-like syndrome, and mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (one patient). The length and location of...
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