Output details
1 - Clinical Medicine
University College London
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Output 0 of 0 in the submission
Article title
SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype.
Type
D - Journal article
Title of journal
J Med Genet
Article number
-
Volume number
46
Issue number
7
First page of article
431
ISSN of journal
1468-6244
Year of publication
2009
URL
-
Number of additional authors
10
Additional information
The author made a substantial contribution to carrying out the study (including acquisition of study data) and to the analysis and interpretation of study data. The author helped critique the output for important intellectual content.
Interdisciplinary
-
Cross-referral requested
-
Research group
None
Citation count
39
Proposed double-weighted
No
Double-weighted statement
-
Reserve for a double-weighted output
No
Non-English
No
English abstract
-
