Progranulin mutations in Dutch familial frontotemporal lobar degeneration-Reference-Cited by-同舟云学术

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Progranulin mutations in Dutch familial frontotemporal lobar degeneration

Published:2007-01-17 Issue:3 Volume:15 Page:369-374
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Bronner Iraad F,Rizzu Patrizia,Seelaar Harro,van Mil Saskia E,Anar Burcu,Azmani Asma,Kaat Laura Donker,Rosso Sonia,Heutink Peter,van Swieten John C

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/5201772.pdf

Reference21 articles.

1. Neary D, Snowden JS, Gustafson L et al: Frontotemporal lobar degeneration – a consensus on clinical diagnostic criteria. Neurology 1998; 51: 1546–1554.

2. Forman MS, Farmer J, Johnson JK et al: Frontotemporal dementia: clinicopathological correlations. Ann Neurol 2006; 59: 952–962.

3. McKhann GM, Albert MS, Grossman M, Miller B, Dickson D, Trojanowski JQ : Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease. Arch Neurol 2001; 58: 1803–1809.

4. Rosso SM, Kamphorst W, de Graaf B et al: Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q2l-22. Brain 2001; 124: 1948–1957.

5. Skibinski G, Parkinson NJ, Brown JM et al: Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia. Nat Genet 2005; 37: 806–808.

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4. Genotype–phenotype links in frontotemporal lobar degeneration;Nature Reviews Neurology;2018-05-18

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