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

Daniel Rabier, C. Diry, Agnès Rötig, Pierre Rustin, Bénédicte Héron, J Bardet, P Parvy, G Ponsot, C. Marsac, J. M. Saudubray,

Journal of Inherited Metabolic Disease · 1998 · 26 citations · 5 references

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