Published in
Oxford University Press (OUP), Human Molecular Genetics, 17(25), p. 3741-3753
DOI: 10.1093/hmg/ddw220
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Loss-of-function mutations in theSIGMAR1gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+signalling
Journal article published in 2016 by
Elisa Gregianin,
Giorgia Pallafacchina,
Sofia Zanin,
Valeria Crippa,
Paola Rusmini,
Angelo Poletti,
Mingyan Fang 
,
Zhouxuan Li,
Laura Diano,
Antonio Petrucci,
Ludovico Lispi,
Tiziana Cavallaro,
Gian M. Fabrizi,
Maria Muglia,
Francesca Boaretto
and other authors.
,
Zhouxuan Li,
Laura Diano,
Antonio Petrucci,
Ludovico Lispi,
Tiziana Cavallaro,
Gian M. Fabrizi,
Maria Muglia,
Francesca Boaretto
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
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