Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy
- Submitting institution
-
St. George's Hospital Medical School
- Unit of assessment
- 1 - Clinical Medicine
- Output identifier
- 154221
- Type
- D - Journal article
- DOI
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10.1016/j.ajhg.2016.06.026
- Title of journal
- AMERICAN JOURNAL OF HUMAN GENETICS
- Article number
- -
- First page
- 735
- Volume
- 99
- Issue
- 3
- ISSN
- 0002-9297
- Open access status
- Deposit exception
- Month of publication
- August
- Year of publication
- 2016
- URL
-
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000383114800019&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=3511c51bff905dacd4
- Supplementary information
-
-
- Request cross-referral to
- -
- Output has been delayed by COVID-19
- No
- COVID-19 affected output statement
- -
- Forensic science
- No
- Criminology
- No
- Interdisciplinary
- No
- Number of additional authors
-
32
- Research group(s)
-
-
- Citation count
- 46
- Proposed double-weighted
- No
- Reserve for an output with double weighting
- No
- Additional information
- -
- Author contribution statement
- -
- Non-English
- No
- English abstract
- -
