(Q38981465)

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The Arg98Trp mutation in human VKORC1 causing VKCFD2 disrupts a di-arginine-based ER retention motif

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The Arg98Trp mutation in human VKORC1 causing VKCFD2 disrupts a di-arginine-based ER retention motif (English)

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8 September 2017

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Katrin J Czogalla

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Simone Rost

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Matthias Watzka

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Johannes Oldenburg

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24 June 2014

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8 September 2017

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124

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8

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1354-1362

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(Q38981465)

The Arg98Trp mutation in human VKORC1 causing VKCFD2 disrupts a di-arginine-based ER retention motif

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