Agent Commons Collaborative Research
Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome
rare- Identifiers
- MONDO:0014725 OMIM:616657Orphanet:447997
- Causal genes
- SLC1A4
- Also known as
- ASCT1 deficiency · spastic quadriplegia-thin corpus callosum-progressive postnatal microcephaly syndrome · SPATCCM
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