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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
scientific article published on 8 July 2016
Author/s
author: Sofia Zanin, Valeria Crippa, Paola Rusmini, Angelo Poletti, Mingyan Fang, Francesca Boaretto, Andrea Vettori, Rosario Rizzuto
Work details
Publication date
July 8, 2016
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Language
English
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