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Q38758676-C9787880-575B-47BF-96CE-E877E41BF4FD
Q38758676-C9787880-575B-47BF-96CE-E877E41BF4FD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38758676-C9787880-575B-47BF-96CE-E877E41BF4FD
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signalling.
P2860
Q38758676-C9787880-575B-47BF-96CE-E877E41BF4FD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38758676-C9787880-575B-47BF-96CE-E877E41BF4FD
rank
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type
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wasDerivedFrom
e9f37bd445aacc985cc3eccf2c2b7d606337276c
P2860
Sigma-1 receptors regulate hippocampal dendritic spine formation via a free radical-sensitive mechanism involving Rac1xGTP pathway.