Output details
4 - Psychology, Psychiatry and Neuroscience
University of Leeds
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Output 0 of 0 in the submission
Article title
Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration
Type
D - Journal article
DOI
Title of journal
Nature Genetics
Article number
-
Volume number
44
Issue number
9
First page of article
1035
ISSN of journal
10614036
Year of publication
2012
URL
-
Number of additional authors
32
Additional information
The author made a substantial contribution to the conception and design of the study.
The author made a substantial contribution to the organisation and conduct of the study.
The author made a substantial contribution to analysis and interpretation of study data.
The author helped draft the output.
The author helped critique the output for important intellectual content.
Interdisciplinary
-
Cross-referral requested
-
Research group
None
Citation count
15
Proposed double-weighted
No
Double-weighted statement
-
Reserve for a double-weighted output
No
Non-English
No
English abstract
-