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Q37458493-74FFF89E-A757-4AB8-A73D-E4B8AD19C1D6
Q37458493-74FFF89E-A757-4AB8-A73D-E4B8AD19C1D6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37458493-74FFF89E-A757-4AB8-A73D-E4B8AD19C1D6
Ca2+ dysregulation in Ryr1(I4895T/wt) mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods
P2860
Q37458493-74FFF89E-A757-4AB8-A73D-E4B8AD19C1D6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37458493-74FFF89E-A757-4AB8-A73D-E4B8AD19C1D6
rank
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type
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wasDerivedFrom
0b1f07eacbb3202c7c39c44d8cdb994fd56ef3f7
P2860
A mutation in Orai1 causes immune deficiency by abrogating CRAC channel function