Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia-Reference-Cited by-同舟云学术

Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia

Published:2008-01-08 Issue:4 Volume:29 Page:512-521
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Mukherjee Odity,Wang Jun,Gitcho Michael,Chakraverty Sumi,Taylor-Reinwald Lisa,Shears Shantia,Kauwe John S.K.,Norton Joanne,Levitch Denise,Bigio Eileen H.,Hatanpaa Kimmo J.,White Charles L.,Morris John C.,Cairns Nigel J.,Goate Alison

Funder

McDonnell Center for Molecular and Cellular Neurobiology

Barnes Jewish Foundation

Washington University Genome Sequencing Center

Winspear Family Center for Research on the Neuropathology of Alzheimer's Disease

McCune Foundation (UTSW)

National Institute on Aging (NIA)

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference24 articles.

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3. Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation;Behrens;Alzheimer Dis Assoc Disord,2007

4. Clinicopathologic studies in cognitively healthy aging and Alzheimer's disease: relation of histologic markers to dementia severity, age, sex, and apolipoprotein E genotype;Berg;Arch Neurol,1998

5. TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions;Cairns;Am J Pathol,2007a

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