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Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia. [electronic resource] by
- Huang, Lijia
- Chardon, Jodi Warman
- Carter, Melissa T
- Friend, Kathie L
- Dudding, Tracy E
- Schwartzentruber, Jeremy
- Zou, Ruobing
- Schofield, Peter W
- Douglas, Stuart
- Bulman, Dennis E
- Boycott, Kym M
Producer: 20130621
In:
Orphanet journal of rare diseases vol. 7
Availability: No items available.
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