Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies - Concepedia

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Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies

DOI Full Paper Access

117

Citations

27

References

2011

Year

Laura Southgate, Rajiv D. Machado, Katie Snape, Martin Primeau, Dimitra Dafou, Deborah Ruddy, Peter Branney, Malcolm E Fisher, Grace J. Lee, Michael A. Simpson,

The American Journal of Human Genetics

Limb AnomaliesSignal TransductionSignaling PathwayGenetic DisorderCdc42/rac1 Gtpase RegulatorGeneticsGain-of-function MutationsMedicineCell BiologyCell Signaling

References

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