Output details
1 - Clinical Medicine
Newcastle University
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Output 0 of 0 in the submission
Article title
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: A novel disorder of mtDNA maintenance
Type
D - Journal article
Title of journal
Brain
Article number
-
Volume number
131
Issue number
2
First page of article
329
ISSN of journal
1460-2156
Year of publication
2008
Number of additional authors
13
Additional information
The author made a substantial contribution to carrying out the study (including acquisition of study data), to analysis and interpretation of study data, and the author helped critique the output for important intellectual content.
Interdisciplinary
-
Cross-referral requested
-
Research group
J - Mitochondrial Disease
Citation count
142
Proposed double-weighted
No
Double-weighted statement
-
Reserve for a double-weighted output
No
Non-English
No
English abstract
-
