fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 3 (Q60195358)

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fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency that has material basis in homozygous mutation in the COA5 gene on chromosome 2q11
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fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 3
fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency that has material basis in homozygous mutation in the COA5 gene on chromosome 2q11

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