Cite
MLA Citation
Jaime Vengoechea et al.. “Clinical variability and female penetrance in X-linked familial FTD/ALS caused by a P506S mutation in UBQLN2.” Amyotrophic lateral sclerosis and frontotemporal degeneration, vol. 14, no. 7, 2013, pp. 615–619. http://access.bl.uk/ark:/81055/vdc_100044730874.0x000001