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Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects. [electronic resource] by
- Seong, Eunju
- Insolera, Ryan
- Dulovic, Marija
- Kamsteeg, Erik-Jan
- Trinh, Joanne
- Brüggemann, Norbert
- Sandford, Erin
- Li, Sheng
- Ozel, Ayse Bilge
- Li, Jun Z
- Jewett, Tamison
- Kievit, Anneke J A
- Münchau, Alexander
- Shakkottai, Vikram
- Klein, Christine
- Collins, Catherine A
- Lohmann, Katja
- van de Warrenburg, Bart P
- Burmeister, Margit
Producer: 20190812
In:
Annals of neurology vol. 83
Availability: No items available.
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