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Characterization of two mutations in the SPTLC1 subunit of serine palmitoyltransferase associated with hereditary sensory and autonomic neuropathy type I. [electronic resource] by
- Rotthier, Annelies
- Penno, Anke
- Rautenstrauss, Bernd
- Auer-Grumbach, Michaela
- Stettner, Georg M
- Asselbergh, Bob
- Van Hoof, Kim
- Sticht, Heinrich
- Lévy, Nicolas
- Timmerman, Vincent
- Hornemann, Thorsten
- Janssens, Katrien
Producer: 20110919
In:
Human mutation vol. 32
Availability: No items available.
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