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MIM:613908 - SPINOCEREBELLAR ATAXIA 35; SCA35
Xenbase Genes: tgm6
Human Disease Resource: MIM
| MONDO:0013485 - spinocerebellar ataxia type 35 |
| DOID:0050982 - spinocerebellar ataxia 35 |
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| MONDO:0013485 - spinocerebellar ataxia type 35 |
| DOID:0050982 - spinocerebellar ataxia 35 |