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Q34478102-1D84F15E-EE39-4750-9DB8-5A4C6D14504C
Q34478102-1D84F15E-EE39-4750-9DB8-5A4C6D14504C
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http://www.wikidata.org/entity/statement/Q34478102-1D84F15E-EE39-4750-9DB8-5A4C6D14504C
Allele-specific gene silencing in two mouse models of autosomal dominant skeletal myopathy.
P2860
Q34478102-1D84F15E-EE39-4750-9DB8-5A4C6D14504C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34478102-1D84F15E-EE39-4750-9DB8-5A4C6D14504C
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wasDerivedFrom
f1c795ff8723c42304638372fe0fa2c53b542145
P2860
Ca2+ dysregulation in Ryr1(I4895T/wt) mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods