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Q54312087-B214CE84-30E3-4D79-974B-31A6A9CDF65B
Q54312087-B214CE84-30E3-4D79-974B-31A6A9CDF65B
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Statement
http://www.wikidata.org/entity/statement/Q54312087-B214CE84-30E3-4D79-974B-31A6A9CDF65B
Clinical features and ryanodine receptor type 1 gene mutation analysis in a Chinese family with central core disease.
P2860
Q54312087-B214CE84-30E3-4D79-974B-31A6A9CDF65B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54312087-B214CE84-30E3-4D79-974B-31A6A9CDF65B
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wasDerivedFrom
eecaa6ccf2842a1ba42ecda3629145b3d2395c2f
P2860
Ca2+ dysregulation in Ryr1(I4895T/wt) mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods