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DDX060
DDX060
http://dx.doi.org/10.1093/HMG/DDX060
A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions.
P356
Q33622482-F4F97E04-B19D-47ED-BD6C-919F739C4909
P356
DDX060
http://dx.doi.org/10.1093/HMG/DDX060