Frontotemporal lobar degeneration genome wide association study replication confirms a risk locus shared with amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

Frontotemporal lobar degeneration genome wide association study replication confirms a risk locus shared with amyotrophic lateral sclerosis

Published:2011-04 Issue:4 Volume:32 Page:758.e1-758.e7
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Rollinson Sara,Mead Simon,Snowden Julie,Richardson Anna,Rohrer Jonathan,Halliwell Nicola,Usher Suzanne,Neary David,Mann David,Hardy John,Pickering-Brown Stuart

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience

Reference28 articles.

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2. Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family;Boxer;J Neurol Neurosurg Psychiatry,2010

3. CHMP2B mutations are not a common cause of frontotemporal lobar degeneration;Cannon;Neurosci Lett,2006

4. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21;Cruts;Nature,2006

5. The structure of haplotype blocks in the human genome;Gabriel;Science,2002

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