D-glyceric aciduria is caused by genetic deficiency of D-glycerate kinase (GLYCTK)

Author:

Sass Jörn Oliver,Fischer Kathleen,Wang Raymond,Christensen Ernst,Scholl-Bürgi Sabine,Chang Richard,Kapelari Klaus,Walter Melanie

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference29 articles.

1. D(+)-glyceric aciduria: etiology and clinical consequences;Bonham;Pediatr Res,1990

2. Hyperglycericacidaemia with hyperglycinaemia: a new inborn error of metabolism;Brandt;Br Med J,1974

3. D-glyceric-acidaemia and non-ketotic hyperglycinaemia. Clinical and laboratory findings in a new syndrome;Brandt;Acta Paediatr Scand,1976

4. L-Glyceric aciduria (primary hyperoxaluria type 2) in siblings in two unrelated families;Chalmers;J Inherit Metab Dis,1984

5. Detecting polymorphisms and mutations in candidate genes;Collins;Am J Hum Genet,2002

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