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Digitale Medien

Non-ketotic hyperglycinaemia: clinical and biochemical aspects (1987)

Tada, K. ; Hayasaka, K.

Springer

European journal of pediatrics 146 (1987), S. 221-227

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ISSN: 1432-1076

Schlagwort(e): Non-ketotic hyperglycinaemia ; Glycine cleavage enzyme

Quelle: Springer Online Journal Archives 1860-2000

Thema: Medizin

Notizen: 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.

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1007/BF00716464

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