ScienceOpen:
research and publishing network
For Publishers
Discovery
Metadata
Peer review
Hosting
Publishing
For Researchers
Join
Publish
Review
Collect
My ScienceOpen
Sign in
Register
Dashboard
Blog
About
Search
Advanced search
My ScienceOpen
Sign in
Register
Dashboard
Search
Search
Advanced search
For Publishers
Discovery
Metadata
Peer review
Hosting
Publishing
For Researchers
Join
Publish
Review
Collect
Blog
About
2
views
0
references
Top references
cited by
1
0 reviews
Review
0
comments
Comment
0
recommends
+1
Recommend
0
collections
Add to
0
shares
Share
Twitter
Sina Weibo
Facebook
Email
5,791
similar
All similar
Record
: found
Abstract
: not found
Article
: not found
Homozygous nonsense mutation in SYNJ1 associated with intractable epilepsy and tau pathology
Author(s):
Publication date:
2014
Journal:
Neurobiol. Aging
Read this article at
ScienceOpen
Bookmark
There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.
Related collections
ScienceOpen Research
Data availability:
Comments
Comment on this article
Sign in to comment
Similar content
5,791
Assignment of SYNJ1 to human chromosome 21q22.2 and Synj12 to the murine homologous region on chromosome 16C3-4 by in situ hybridization.
Authors:
O Cremona
,
M Nimmakayalu
,
J Haffner
…
Non-motor symptoms and cardiac innervation in SYNJ1-related parkinsonism.
Authors:
L Santoro
,
L Bilo
,
A Cuocolo
…
Down Syndrome Fetal Fibroblasts Display Alterations of Endosomal Trafficking Possibly due to SYNJ1 Overexpression
Authors:
Laura De Rosa
,
Dominga Fasano
,
Lucrezia Zerillo
…
See all similar
Cited by
1
PIPs in neurological diseases
Authors:
Mark G. Waugh
See all cited by