(Q26492812)

English

mitochondrial complex III deficiency nuclear type 8

mitochondrial complex III deficiency characterized by childhood onset of progressive neurodegeneration that has material basis in homozygous mutation in the LYRM7 gene on chromosome 5q23

  • MC3DN8
  • MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8
  • MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8

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