Mutations in TUBB4A and spastic paraplegia

Mov Disord. 2015 Nov;30(13):1857-8. doi: 10.1002/mds.26444. Epub 2015 Oct 19.

Authors

Kishore R Kumar^{1

2}, Franca Vulinovic³, Katja Lohmann³, Jin-Sung Park¹, Susen Schaake³, Carolyn M Sue¹, Christine Klein³

Affiliations

¹ Department of Neurogenetics, Kolling Institute of Medical Research and Royal North Shore Hospital, The University of Sydney, Australia.
² Kinghorn Centre for Clinical Genomics, Garvan Institute of Medical Research, Darlinghurst, Sydney, Australia.
³ Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.

PMID: 26477786
DOI: 10.1002/mds.26444

No abstract available

Publication types

Letter
Research Support, Non-U.S. Gov't
Comment

MeSH terms

Female
Genes, Dominant*
Humans
Male
Mosaicism*
Spastic Paraplegia, Hereditary / genetics*
Spastic Paraplegia, Hereditary / physiopathology*
Tubulin / genetics*

Substances

Tubulin