Pages that link to "Q33986374"
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The following pages link to Glycine decarboxylase mutations: a distinctive phenotype of nonketotic hyperglycinemia in adults (Q33986374):
Displaying 14 items.
- Rapid diagnosis of glycine encephalopathy by 13C-glycine breath test (Q28236196) (← links)
- The pediatric neurotransmitter disorders (Q28240100) (← links)
- Comprehensive mutation analysis of GLDC, AMT, and GCSH in nonketotic hyperglycinemia (Q28294916) (← links)
- Glycine receptors support excitatory neurotransmitter release in developing mouse visual cortex (Q28512097) (← links)
- Psychiatric manifestations revealing inborn errors of metabolism in adolescents and adults (Q34005690) (← links)
- Biochemical and molecular predictors for prognosis in nonketotic hyperglycinemia (Q36618764) (← links)
- Two novel laboratory tests facilitating diagnosis of glycine encephalopathy (nonketotic hyperglycinemia) (Q37862429) (← links)
- Treatable inborn errors of metabolism causing neurological symptoms in adults (Q38178697) (← links)
- Genomic deletion within GLDC is a major cause of non-ketotic hyperglycinaemia (Q41108615) (← links)
- Delivery of a normal baby after preimplantation genetic diagnosis for non-ketotic hyperglycinaemia (Q46543602) (← links)
- Model mice for mild-form glycine encephalopathy: behavioral and biochemical characterizations and efficacy of antagonists for the glycine binding site of N-methyl D-aspartate receptor (Q46643375) (← links)
- Contribution of CSF analysis to the diagnosis of inborn errors of metabolism in adult patients (Q46886244) (← links)
- Treatable hereditary neuro-metabolic diseases (Q46886261) (← links)
- Diagnosis and treatment of neurotransmitter disorders (Q79219450) (← links)