Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation-Reference-Cited by-同舟云学术

Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation

Published:2009-05 Issue:5 Volume:30 Page:752-758
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Bersano Anna,Del Bo Roberto,Lamperti Costanza,Ghezzi Serena,Fagiolari Gigliola,Fortunato Francesco,Ballabio Elena,Moggio Maurizio,Candelise Livia,Galimberti Daniela,Virgilio Roberta,Lanfranconi Silvia,Torrente Yvan,Carpo Marinella,Bresolin Nereo,Comi Giacomo P.,Corti Stefania

Publisher

Elsevier BV

Subject

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

Reference19 articles.

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

2. Critically ill patients: immunological evidence of inflammation in muscle biopsy;Bazzi;Clin. Neuropathol.,1999

3. The apolipoprotein E epsilon4 allele causes a faster decline of cognitive performances in Down's syndrome subjects;Del Bo;J. Neurol. Sci.,1997

4. Novel missense mutation and large deletion of GNE gene in autosomal-recessive inclusion body myopathy;Del Bo;Muscle Nerve,2003

5. Complete structure of p97/valosin-containing protein reveals communication between nucleotide domains;DeLaBarre;Nat. Struct. Biol.,2003

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