(Q26492813)

English

mitochondrial complex III deficiency nuclear type 9

mitochondrial complex III deficiency that has material basis in homozygous mutation in the UQCC3 gene on chromosome 11q12

  • MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9; MC3DN9
  • MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9
  • MC3DN9

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