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Q34478102-AC5E1230-9FD3-40C9-843B-AAAB33EAFDCC
Q34478102-AC5E1230-9FD3-40C9-843B-AAAB33EAFDCC
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http://www.wikidata.org/entity/statement/Q34478102-AC5E1230-9FD3-40C9-843B-AAAB33EAFDCC
Allele-specific gene silencing in two mouse models of autosomal dominant skeletal myopathy.
P2860
Q34478102-AC5E1230-9FD3-40C9-843B-AAAB33EAFDCC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34478102-AC5E1230-9FD3-40C9-843B-AAAB33EAFDCC
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wasDerivedFrom
f1c795ff8723c42304638372fe0fa2c53b542145
P2860
An Ryr1I4895T mutation abolishes Ca2+ release channel function and delays development in homozygous offspring of a mutant mouse line