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MTDPS7 Dominant: Variable, or incomplete, connections between ataxia & mitochondrial disorders SCA 28 Cerebellar ataxia, Deafness & Narcolepsy OPA1: Occasional patients (ADOAD) AD-PEO: Rare patients RRM2B OGDH X-linked Sideroblastic anemia & Spinocerebellar ataxia (XLSA/A) Other: Variable or Uncertain Deafness: Usually recessive or mitochondrial Leigh's: Usually recessive or mitochondrial CAPOS

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These alternative splice variants have been raised due to the loss or gain of exons or introns, such as OsDJ-1C .1 losses one exon to generate OsDJ-1C .2 and loss of another exon make the second variant OsDJ-1C .3 (Figure S1)