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Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signalling

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Description scientific article published on 8 July 2016
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author: Paola Rusmini  Valeria Crippa  Andrea Vettori  Rosario Rizzuto  Francesca Boaretto  Mingyan Fang  Sofia Zanin  Angelo Poletti 

Publication date July 8, 2016
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