Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies (Q24626495)

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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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    Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies (English)
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    Katie M Snape
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    Martin Primeau
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    Deborah M Ruddy
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    Peter A Branney
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    Grace J Lee
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    Yi He
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    Teisha Y Bradshaw
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    Bettina Blaumeiser
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    William S Winship
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    Willie Reardon
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    Nathalie Lamarche-Vane
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    13 May 2011
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    88
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    5
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    574-85
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