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Output details

1 - Clinical Medicine

Queen Mary University of London

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Output 0 of 0 in the submission
Article title

Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies.

Type
D - Journal article
Title of journal
Am J Hum Genet
Article number
-
Volume number
88
Issue number
5
First page of article
574
ISSN of journal
1537-6605
Year of publication
2011
URL
-
Number of additional authors
20
Additional information
-
Interdisciplinary
-
Cross-referral requested
-
Research group
None
Citation count
24
Proposed double-weighted
No
Double-weighted statement
-
Reserve for a double-weighted output
No
Non-English
No
English abstract
-