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2.1.2.10
medicine
a subset of nonketotic hyperglycinemia cases is due to mutations in the gene for the T-protein
485697
2.1.2.10
medicine
identification of several mutations and polymorphisms occurring in patients with glycine encephalopathy, NKH, and methods for their PCR-restriction enzyme analysis
662879
2.1.2.10
medicine
strategy for molecular investigation of patients with nonketotic hyperglycinemia: defective glycine cleavage enzyme system, composed of P-, H-, T- and L-protein, 15% of patients have a T-protein defect
485696
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