Output details
1 - Clinical Medicine
King's College London
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Output 0 of 0 in the submission
Article title
C-terminal deletions in the ALAS2 gene lead to gain of function and cause X-linked dominant protoporphyria without anemia or iron overload
Type
D - Journal article
Title of journal
American Journal of Human Genetics
Article number
-
Volume number
83
Issue number
3
First page of article
408
ISSN of journal
0002-9297
Year of publication
2008
URL
-
Number of additional authors
17
Additional information
a. The author made a substantial contribution to the organisation of the conduct of the study; to carrying out the study; and to analysis and interpretation of study data.
and
b. The author critique the output for important intellectual content.
Interdisciplinary
-
Cross-referral requested
-
Research group
F - Transplantation
Citation count
60
Proposed double-weighted
No
Double-weighted statement
-
Reserve for a double-weighted output
No
Non-English
No
English abstract
-