Clinical and molecular heterogeneity in patients with mitochondrial encephalomyopathies due to complex I deficiency

J Inherit Metab Dis. 1988;11(3):333-6. doi: 10.1007/BF01800387.

Authors

T Ichiki¹, M Kobayashi, Y Wada, M Tanaka, T Ozawa

Affiliation

¹ Department of Pediatrics, Nagoya City University Medical School, Japan.

PMID: 3148084
DOI: 10.1007/BF01800387

No abstract available

MeSH terms

Blotting, Western
Brain / abnormalities*
Humans
Immunochemistry
Mitochondria, Muscle / enzymology*
NAD(P)H Dehydrogenase (Quinone)
Quinone Reductases / deficiency*

Substances

NAD(P)H Dehydrogenase (Quinone)
Quinone Reductases