Hereditary spastic paraplegia caused by a mutation in the VCP gene

Comment

Susanne T de Bot et al. Brain. 2012 Dec.

. 2012 Dec;135(Pt 12):e223; author reply e224.

doi: 10.1093/brain/aws201. Epub 2012 Sep 18.

No abstract available

Comment in

Hereditary spastic paraplegia type 8: Neuropathological findings.
Pehrson C, Hertz JM, Wirenfeldt M, Stenager E, Wermuth L, Winther Kristensen B. Pehrson C, et al. Brain Pathol. 2018 Mar;28(2):292-294. doi: 10.1111/bpa.12494. Brain Pathol. 2018. PMID: 28181327 Free PMC article. No abstract available.

Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases.
Clemen CS, Tangavelou K, Strucksberg KH, Just S, Gaertner L, Regus-Leidig H, Stumpf M, Reimann J, Coras R, Morgan RO, Fernandez MP, Hofmann A, Müller S, Schoser B, Hanisch FG, Rottbauer W, Blümcke I, von Hörsten S, Eichinger L, Schröder R. Clemen CS, et al. Brain. 2010 Oct;133(10):2920-41. doi: 10.1093/brain/awq222. Epub 2010 Sep 9. Brain. 2010. PMID: 20833645