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Q34439584-13131F79-735C-4329-9E27-DDB48A1215DC
Q34439584-13131F79-735C-4329-9E27-DDB48A1215DC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34439584-13131F79-735C-4329-9E27-DDB48A1215DC
Muscle weakness in Ryr1I4895T/WT knock-in mice as a result of reduced ryanodine receptor Ca2+ ion permeation and release from the sarcoplasmic reticulum.
P2860
Q34439584-13131F79-735C-4329-9E27-DDB48A1215DC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34439584-13131F79-735C-4329-9E27-DDB48A1215DC
rank
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type
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wasDerivedFrom
4b96c488b2ac3b498f55daf9eb0275a565551d6b
P2860
A homozygous splicing mutation causing a depletion of skeletal muscle RYR1 is associated with multi-minicore disease congenital myopathy with ophthalmoplegia.