A novel deletion in progranulin gene is associated with FTDP-17 and CBS-Reference-Cited by-同舟云学术

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A novel deletion in progranulin gene is associated with FTDP-17 and CBS

Published:2008-03 Issue:3 Volume:29 Page:427-435
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Benussi Luisa,Binetti Giuliano,Sina Elena,Gigola Lara,Bettecken Thomas,Meitinger Thomas,Ghidoni Roberta

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Clinical Neurology,Ageing,General Neuroscience

Reference51 articles.

1. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17;Baker;Nature,2006

2. Granulins: the structure and function of an emerging family of growth factors;Bateman;J. Endocrinol.,1998

3. Isolation and sequence of the granulin precursor cDNA from human bone marrow reveals tandem cysteine-rich granulin domains;Bhandari;Proc. Natl. Acad. Sci. U.S.A.,1992

4. Prevalence of TAU mutations in an Italian clinical series of familial frontotemporal patients;Binetti;Neurosci. Lett.,2003

5. A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L);Bird;Brain,1999

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