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

Autor: Wijburg FA; Department of Pediatrics, University Hospital of Amsterdam, The Netherlands., Barth PG, Ruitenbeek W, Wanders RJ, Vos GD, Ploos van Amstel SL, Schutgens RB
Jazyk: angličtina
Zdroj: Journal of inherited metabolic disease [J Inherit Metab Dis] 1989; Vol. 12 Suppl 2, pp. 349-51.
DOI: 10.1007/BF03335419
Databáze: MEDLINE
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