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Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia. [electronic resource] by
- Pérez-Brangulí, Francesc
- Mishra, Himanshu K
- Prots, Iryna
- Havlicek, Steven
- Kohl, Zacharias
- Saul, Domenica
- Rummel, Christine
- Dorca-Arevalo, Jonatan
- Regensburger, Martin
- Graef, Daniela
- Sock, Elisabeth
- Blasi, Juan
- Groemer, Teja W
- Schlötzer-Schrehardt, Ursula
- Winkler, Jürgen
- Winner, Beate
Producer: 20150423
In:
Human molecular genetics vol. 23
Availability: No items available.
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