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Case Reports

. 1989:12 Suppl 2:349-51.

doi: 10.1007/BF03335419.

Familial NADH: Q1 oxidoreductase (complex I) deficiency: variable expression and possible treatment

F A Wijburg¹, P G Barth, W Ruitenbeek, R J Wanders, G D Vos, S L Ploos van Amstel, R B Schutgens

Affiliations

PMID: 2512441
DOI: 10.1007/BF03335419

Case Reports

Familial NADH: Q1 oxidoreductase (complex I) deficiency: variable expression and possible treatment

F A Wijburg et al. J Inherit Metab Dis. 1989.

. 1989:12 Suppl 2:349-51.

doi: 10.1007/BF03335419.

Authors

F A Wijburg¹, P G Barth, W Ruitenbeek, R J Wanders, G D Vos, S L Ploos van Amstel, R B Schutgens

Affiliation

¹ Department of Pediatrics, University Hospital of Amsterdam, The Netherlands.

PMID: 2512441
DOI: 10.1007/BF03335419

No abstract available

PubMed Disclaimer

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References

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1. Eur J Pediatr. 1986 Feb;144(5):441-4 - PubMed
1. Lancet. 1983 Sep 3;2(8349):581-2 - PubMed
1. J Neurol Sci. 1981 Sep;51(3):371-82 - PubMed

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