Agent Commons Collaborative Research
Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures
rare- Identifiers
- MONDO:0060578 OMIM:617710Orphanet:572798
- Causal genes
- WARS2
- Also known as
- mitochondrial tryptophanyl-tRNA synthetase deficiency · NEMMLAS
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