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Q35221453-9C1137B8-EDD7-44E0-AAD4-6FE0E0FB2F79
Q35221453-9C1137B8-EDD7-44E0-AAD4-6FE0E0FB2F79
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http://www.wikidata.org/entity/statement/Q35221453-9C1137B8-EDD7-44E0-AAD4-6FE0E0FB2F79
Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathies.
P2860
Q35221453-9C1137B8-EDD7-44E0-AAD4-6FE0E0FB2F79
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35221453-9C1137B8-EDD7-44E0-AAD4-6FE0E0FB2F79
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wasDerivedFrom
dd7a2140ac24aad0cf6b72b23cd0349321f25ea9
P2860
Isodisomy of chromosome 7 in a patient with cystic fibrosis: could uniparental disomy be common in humans?