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Q37458493-0EDAEE99-5167-4333-A54F-3D3418A524AA
Q37458493-0EDAEE99-5167-4333-A54F-3D3418A524AA
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http://www.wikidata.org/entity/statement/Q37458493-0EDAEE99-5167-4333-A54F-3D3418A524AA
Ca2+ dysregulation in Ryr1(I4895T/wt) mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods
P2860
Q37458493-0EDAEE99-5167-4333-A54F-3D3418A524AA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37458493-0EDAEE99-5167-4333-A54F-3D3418A524AA
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wasDerivedFrom
0b1f07eacbb3202c7c39c44d8cdb994fd56ef3f7
P2860
An Ryr1I4895T mutation abolishes Ca2+ release channel function and delays development in homozygous offspring of a mutant mouse line