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

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Description scientific article
Author/s

author: Martin Zenker  Laura Southgate  Rajiv Machado  Wim Wuyts  Dimitra Dafou  David FitzPatrick  Malcolm E Fisher  Eamonn R Maher  Bettina Blaumeiser  Michael Simpson  Richard C Trembath 

Publication date May 13, 2011
Language English
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