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Study of Phosphatidylcholine in a Patient With Methionine Adenosyltransferase Deficiency
This study has been completed.
Study NCT00006061   Information provided by Office of Rare Diseases (ORD)
First Received: July 5, 2000   Last Updated: June 23, 2005   History of Changes
Related Studies can be found by searching for the Conditions, Interventions, and Sponsors found in this study:
Conditions listed in this trial
Metabolism, Inborn Errors
More general conditions related to this trial
Genetic Diseases, Inborn
Metabolic Diseases
Interventions listed in this trial
phosphatidylcholine
Sponsors listed in this trial
National Center for Research Resources (NCRR)
UNC Lineberger Comprehensive Cancer Center


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