Inborn defects of the mitochondrial portion of the urea cycle
- PMID: 3555250
- DOI: 10.1111/j.1749-6632.1986.tb46551.x
Inborn defects of the mitochondrial portion of the urea cycle
Similar articles
-
[Molecular genetics of urea cycle diseases].Seikagaku. 1990 Sep;62(9):1170-7. Seikagaku. 1990. PMID: 2258657 Japanese. No abstract available.
-
Diagnosis of urea cycle disorders.Ann Clin Biochem. 1977 May;14(3):136-8. doi: 10.1177/000456327701400128. Ann Clin Biochem. 1977. PMID: 17345 No abstract available.
-
Urea cycle enzymopathies.Semin Liver Dis. 1982 Nov;2(4):329-39. doi: 10.1055/s-2008-1040719. Semin Liver Dis. 1982. PMID: 6763345 Review. No abstract available.
-
Genetic approach to prenatal diagnosis in urea cycle defects.Prenat Diagn. 2004 May;24(5):378-83. doi: 10.1002/pd.884. Prenat Diagn. 2004. PMID: 15164414
-
Urea biosynthesis II. Normal and abnormal regulation.Am J Clin Nutr. 1978 Jan;31(1):126-33. doi: 10.1093/ajcn/31.1.126. Am J Clin Nutr. 1978. PMID: 339704 Review. No abstract available.
Cited by
-
Changes in brain mitochondrial bioenergetics in protein-deficient rats.Br J Exp Pathol. 1989 Dec;70(6):607-19. Br J Exp Pathol. 1989. PMID: 2513864 Free PMC article.
-
Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease.J Am Heart Assoc. 2019 May 21;8(10):e011922. doi: 10.1161/JAHA.119.011922. J Am Heart Assoc. 2019. PMID: 31070104 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources