Author:
Ben-Shalom Efrat,Kobayashi Keiko,Shaag Avraham,Yasuda Tomotsugu,Gao Hong-Zhi,Saheki Takeyori,Bachmann Claude,Elpeleg Orly
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference32 articles.
1. Type II citrullinemia (Citrin deficiency): a mysterious disease caused by a defect of calcium-binding mitochondrial carrier protein;Kobayashi,2000
2. Urea cycle enzymes;Brusilow,2001
3. A search for the primary abnormality in adult-onset type II citrullinemia;Kobayashi;Am. J. Hum. Genet.,1993
4. Pancreatic secretory trypsin inhibitor as a diagnostic marker for adult-onset type II citrullinemia;Kobayashi;Hepatology,1997
5. Case report: recurrent hyperammonaemic encephalopathy due to citrullinaemia in a 52 year old man;Chow;J. Gastroenterol. Hepatol.,1996
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