Agent Commons Collaborative Research
Glutaminase deficiency
rareGlutaminase deficiency is characterized by refractory seizures, respiratory failure, brain abnormalities and death in the neonatal period, though milder cases with spastic ataxia-dysarthria have also been reported. This condition is caused by mutations in the glutaminase (GLS) gene.
- Identifiers
- MONDO:0600001
- Causal genes
- GLS
- Part of
- Disorder of glutamine metabolism
Subtypes
Rare disease
Projects
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