A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series

J. Beck, J.D. Rohrer, T. Campbell, A. Isaacs, K.E. Morrison, E.F. Goodall, E.K. Warrington, J. Stevens, T. Revesz, J. Holton, S. Al-Sarraj, A. King, R. Scahill, J.D. Warren, N.C. Fox, M.N. Rossor, J. Collinge, S. Mead

Research output: Contribution to journalArticle

176 Citations (Scopus)
Original languageEnglish
Pages (from-to)706-720
Number of pages15
JournalBrain
Volume131
Issue number3
DOIs
Publication statusPublished - 01 Mar 2008

Cite this

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), 706-720. https://doi.org/10.1093/brain/awm320