The treatment of congenital lactic acidoses
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01799117
Reference44 articles.
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3. Arnold DL, Taylor DJ, Radda GK (1985) Investigation of human mitochondrial myopathies by phosphorus magnetic resonance spectroscopy.Ann Neurol 18: 189–196.
4. Arts WF, Scholte HR, Bogaard JM, Kerrebijn KG, Luyt-Houwen IE (1983) NADH-CoQ reductase deficient myopathy: successful treatment with riboflavin.Lancet 2: 581–582.
5. Bakker HD, Scholte HR, Jeneson JA, Busch HF, Abeling NG, van Gennip AH (1994) Vitamin-responsive complex I deficiency in a myopathic patient with increased activity of the terminal respiratory chain and lactic acidosis.J Inher Metab Dis 17: 196–204.
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