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Q35221453-CCA96177-28A0-4681-A791-91967967604D
Q35221453-CCA96177-28A0-4681-A791-91967967604D
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Statement
http://www.wikidata.org/entity/statement/Q35221453-CCA96177-28A0-4681-A791-91967967604D
Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathies.
P2860
Q35221453-CCA96177-28A0-4681-A791-91967967604D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35221453-CCA96177-28A0-4681-A791-91967967604D
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wasDerivedFrom
dd7a2140ac24aad0cf6b72b23cd0349321f25ea9
P2860
A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome.