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Related Experiment Videos

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

D Rabier1, C Diry, A Rotig

  • 1Laboratoire Biochimie B, Hôpital Necker-Enfants Malades, Paris, France.

Journal of Inherited Metabolic Disease
|August 1, 1998
PubMed
Summary

No abstract available in PubMed .

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