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These six phenotypes include Alpers-Huttenlocher syndrome (AHS), ataxia neuropathy spectrum (ANS), myoclonic epilepsy myopathy sensory ataxia (MEMSA), myocerebrohepatopathy spectrum (MCHS), and the progressive external ophthalmoplegias (PEO) that include the autosomal recessive (arPEO) and autosomal dominant (adPEO) forms