Errata (DOI:10.1016/S1474-4422(07)70224-7);Genetic basis of frontotemporal dementia

Lancet Neurology

Volumn 6, Issue 10, 2007, Pages 840-841

  van Swieten, John C ^a  

^a ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

PROGRANULIN; TAU PROTEIN;

FRONTOTEMPORAL DEMENTIA; GENE MUTATION; GENETIC ASSOCIATION; HUMAN; LETTER; PRIORITY JOURNAL;

EID: 34548625293     PISSN: 14744422     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1474-4422(07)70279-X     Document Type: Erratum

References (12)

1. McKhann G., Albert M., Grossman M., Miller B., Dickson D., and Trojanowski J. Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease. Arch Neurol 58 (2001) 1803-1809
2. Hutton M., Lendon C., Rizzu P., et al. Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17. Nature 393 (1998) 702-705
3. van Swieten J., and Spillantini M. Hereditary frontotemporal dementia caused by tau gene mutations. Brain Pathol 17 (2007) 63-73
4. Baker M., Mackenzie I., Pickering-Brown S., et al. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature 442 (2006) 916-919
5. Cruts M., Gijselinck I., van der Zee J., et al. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature 442 (2006) 920-924
6. Le Ber I., van der Zee J., Hannequin D., et al. Progranulin null mutations in both sporadic and familial frontotemporal dementia. Hum Mutat 28 (2007) 846-855
7. Neumann M., Sampathu D., Kwong L., et al. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 314 (2006) 130-133
8. Mackenzie I., Baker M., Pickering-Brown S., et al. The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene. Brain 129 (2006) 3081-3090
9. Snowden J., Pickering-Brown S., Mackenzie I., et al. Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia. Brain 129 (2006) 3091-3102
10. Josephs K., Ahmed Z., Katsuse O., et al. Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations. J Neuropathol Exp Neurol 66 (2007) 142-151
11. Rademakers R., Baker M., Gass J., et al. An international initiative to study phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C→T (Arg493X) mutation. Lancet Neurol 6 (2007) 857-868
12. Bronner I., Rizzu P., Seelaar H., et al. Progranulin mutations in Dutch familial frontotemporal lobar degeneration. Eur J Hum Genet 15 (2007) 369-374