Electronic Resource
Springer
European journal of pediatrics
146 (1987), S. 221-227
ISSN:
1432-1076
Keywords:
Non-ketotic hyperglycinaemia
;
Glycine cleavage enzyme
Source:
Springer Online Journal Archives 1860-2000
Topics:
Medicine
Notes:
Abstracts Non-ketotic hyperglycinaemia is an autosomal recessive disorder of glycine metabolism characterized by elevated concentrations of glycine in plasma, urine and cerebrospinal fluid. The fundamental defect was found to lie in the glycine cleavage system. It is of significance that the major pathway for the catabolism of glycine was elucidated through the studies of hyperglycinaemia. The present knowledge about non-ketotic hyperglycinaemia is described in clinical and biochemical aspects.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/BF00716464
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