ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegia
- Resource Type
- Journal
- Authors
- Bouwkamp, Christian G.; Afawi, Zaid; Fattal-Valevski, Aviva; Krabbendam, Inge E.; Rivetti, Stefano; Masalha, Rafik; Quadri, Marialuisa; Breedveld, Guido J.; Mandel, Hanna; Abu Tailakh, Muhammad; Beverloo, H. Berna; Stevanin, Giovanni; Brice, Alexis; van IJcken, Wilfred F. J.; Vernooij, Meike W.; Dolga, Amalia M.; de Vrij, Femke M. S.; Bonifati, Vincenzo; Kushner, Steven A.
- Source
- NEUROLOGY-GENETICS; APR 2018, 4 2, pe223 9p.
- Subject
- Language
- English
- ISSN
- 23767839