Sustained engraftment and tissue enzyme activity after liver cell
transplantation for argininosuccinate lyase deficiency.
Stephenne X, Najimi M, Sibille C, Nassogne MC, Smets F, Sokal EM.
Hepatocyte transplantation is a promising therapeutic option for various inborn errors of metabolism, as is exemplified by this case report.
For more information on urea cycle defects, please see chapter 85.
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Philippe Campeau, MD
Resident in Medical Genetics at McGill University
OMMBID Blog Administrator