A Point Mutation in the Ubiquitin Ligase RNF170 That Causes Autosomal Dominant Sensory Ataxia Destabilizes the Protein and Impairs Inositol 1,4,5-Trisphosphate Receptor-mediated Ca2+ Signaling (Q35662322)
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scientific article published on 16 April 2015
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English | A Point Mutation in the Ubiquitin Ligase RNF170 That Causes Autosomal Dominant Sensory Ataxia Destabilizes the Protein and Impairs Inositol 1,4,5-Trisphosphate Receptor-mediated Ca2+ Signaling |
scientific article published on 16 April 2015 |
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A Point Mutation in the Ubiquitin Ligase RNF170 That Causes Autosomal Dominant Sensory Ataxia Destabilizes the Protein and Impairs Inositol 1,4,5-Trisphosphate Receptor-mediated Ca2+ Signaling (English)
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Nicolas Dupré
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Forrest A Wright
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Justine P Lu
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Danielle A Sliter
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Richard J H Wojcikiewicz
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16 April 2015
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290
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22
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13948-13957
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