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Persistent hypocitrullinaemia as a marker for mtDNA NARP T 8993 G mutation?

Daniel Rabier,C. Diry,Agnès Rötig,Pierre Rustin,Bénédicte Héron,J Bardet+6 more-1998-06-01-Journal of Inherited Metabolic Disease
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Library scienceHeronGeneticsBiologyComputer scienceEcology

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