| Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
|---|---|---|---|---|---|---|
| 2006 | HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin | Mukherjee, O.; Pastor, P.; Cairns, N. J.; Chakraverty, S.; Kauwe, J. S.; Shears, S.; Behrens, M. I.; Budde, J.; Hinrichs, A. L.; Norton, J.; Levitch, D.; Taylor-Reinwald, L.; Gitcho, M.; Tu, P. H.; Tenenholz Grinberg, L.; Liscic, R. M.; Armendariz, J.; Morris, J. C.; Goate, A. M. | Ann Neurol 60(3), 314-322 |
