Biochemical and molecular predictors for prognosis in nonketotic hyperglycinemia

Innovative strategies to treat protein misfolding in inborn errors of metabolism: pharmacological chaperones and proteostasis regulators

(2014) Ania C. Muntau et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5

(2013) Peter R. Baker et al.   BRAIN

Structure of the Homodimeric Glycine Decarboxylase P-protein fromSynechocystissp. PCC 6803 Suggests a Mechanism for Redox Regulation

(2013) Dirk Hasse et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Prediction of long-term outcome in glycine encephalopathy: a clinical survey

(2011) Julia B. Hennermann et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Late-onset nonketotic hyperglycinemia caused by a novel homozygous missense mutation in the GLDC gene

(2011) Catherine Brunel-Guitton et al.   MOLECULAR GENETICS AND METABOLISM

Clinical, ethical and legal considerations in the treatment of newborns with non-ketotic hyperglycinaemia

(2008) A. Boneh et al.   MOLECULAR GENETICS AND METABOLISM