mitochondrial complex III deficiency nuclear type 8 (Q26492812)
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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| 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 |
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