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. 1985 Sep;35(9):1396-7.
doi: 10.1212/wnl.35.9.1396.

Muscle mitochondria from patients with Duchenne muscular dystrophy have a normal beta oxidation, but an impaired oxidative phosphorylation

H R Scholte, I E Luyt-Houwen, H F Busch, F G Jennekens

Muscle mitochondria from patients with Duchenne muscular dystrophy have a normal beta oxidation, but an impaired oxidative phosphorylation

H R Scholte et al. Neurology. 1985 Sep.
No abstract available

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