CHMP2B mutations are not a cause of dementia in Dutch patients with familial and sporadic frontotemporal dementia-Reference-Cited by-同舟云学术

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CHMP2B mutations are not a cause of dementia in Dutch patients with familial and sporadic frontotemporal dementia

Published:2006 Issue:8 Volume:141B Page:944-946
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Rizzu Patrizia,van Mil Saskia E.,Anar Burcu,Rosso Sonia M.,Kaat Laura Donker,Heutink Peter,van Swieten John C.

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics (clinical)

Reference9 articles.

1. Clinical and neuropathological criteria for frontotemporal dementia. The Lund and Manchester Groups.

2. A Protein's Final ESCRT

3. Chromosome 3-linked frontotemporal dementia

4. CHMP2B mutations are not a common cause of frontotemporal lobar degeneration

5. Linkage of Familial Amyotrophic Lateral Sclerosis With Frontotemporal Dementia to Chromosome 9q21-q22

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1. A novel splice‐site mutation in CHMP2B associated with frontotemporal dementia: The first report from China and literature review;Molecular Genetics & Genomic Medicine;2023-06-05

2. Neuroprotective activity of ursodeoxycholic acid in CHMP2B models of frontotemporal dementia;Neurobiology of Disease;2020-10

3. The role of ESCRT during development and functioning of the nervous system;Seminars in Cell & Developmental Biology;2018-02

4. Frontotemporal dementia;Neurogenetics, Part II;2018

5. A transgenic mouse expressing CHMP2Bintron5mutant in neurons develops histological and behavioural features of amyotrophic lateral sclerosis and frontotemporal dementia;Human Molecular Genetics;2016-06-21

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