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

J Inherit Metab Dis

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

Published: June 1998

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Source
http://dx.doi.org/10.1023/a:1005391300203DOI Listing

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