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Q38758676-9C2A0EDA-5552-4915-B362-EA0952372A9C
Q38758676-9C2A0EDA-5552-4915-B362-EA0952372A9C
BestRank
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http://www.wikidata.org/entity/statement/Q38758676-9C2A0EDA-5552-4915-B362-EA0952372A9C
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signalling.
P2860
Q38758676-9C2A0EDA-5552-4915-B362-EA0952372A9C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38758676-9C2A0EDA-5552-4915-B362-EA0952372A9C
rank
NormalRank
type
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Statement
wasDerivedFrom
e9f37bd445aacc985cc3eccf2c2b7d606337276c
P2860
Copy number variation detection and genotyping from exome sequence data.