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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

Abstract

No abstract available in PubMed .

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