Bibliography
Beck, J., Rohrer, J. D., Campbell, T., Isaacs, A., Morrison, K. E., Goodall, E. F., Warrington, E. K., Stevens, J., Revesz, T., Holton, J., Al-Sarraj, S., King, A., Scahill, R., Warren, J. D., Fox, N. C., Rossor, M. N., Collinge, J., & Mead, S. (2008). A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series. Brain, 131(3), 706â720.
Authors
18
- J. Beck (first)
- J. D. Rohrer (additional)
- T. Campbell (additional)
- A. Isaacs (additional)
- K. E. Morrison (additional)
- E. F. Goodall (additional)
- E. K. Warrington (additional)
- J. Stevens (additional)
- T. Revesz (additional)
- J. Holton (additional)
- S. Al-Sarraj (additional)
- A. King (additional)
- R. Scahill (additional)
- J. D. Warren (additional)
- N. C. Fox (additional)
- M. N. Rossor (additional)
- J. Collinge (additional)
- S. Mead (additional)
Dates
Type | When |
---|---|
Created | 17 years, 7 months ago (Jan. 30, 2008, 3:24 p.m.) |
Deposited | 8 years ago (Aug. 22, 2017, 3:33 p.m.) |
Indexed | 6 days, 1 hour ago (Aug. 26, 2025, 2:51 a.m.) |
Issued | 17 years, 6 months ago (Feb. 7, 2008) |
Published | 17 years, 6 months ago (Feb. 7, 2008) |
Published Online | 17 years, 6 months ago (Feb. 7, 2008) |
@article{Beck_2008, title={A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series}, volume={131}, ISSN={1460-2156}, url={http://dx.doi.org/10.1093/brain/awm320}, DOI={10.1093/brain/awm320}, number={3}, journal={Brain}, publisher={Oxford University Press (OUP)}, author={Beck, J. and Rohrer, J. D. and Campbell, T. and Isaacs, A. and Morrison, K. E. and Goodall, E. F. and Warrington, E. K. and Stevens, J. and Revesz, T. and Holton, J. and Al-Sarraj, S. and King, A. and Scahill, R. and Warren, J. D. and Fox, N. C. and Rossor, M. N. and Collinge, J. and Mead, S.}, year={2008}, month=feb, pages={706–720} }