Autosomal dominant complex hereditary spastic paraplegia due to mutations in Spastin gene (Q100925)
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No description defined
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_92075119 |
||
| English | Autosomal dominant complex hereditary spastic paraplegia due to mutations in Spastin gene |
No description defined |
Statements
CID11:ID_92075119
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dki-india-ID_92075119
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Concluído
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15 August 2026
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