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PubMed:24868377 / 233-334 JSONTXT

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PubTator4TogoVar

Id Subject Object Predicate Lexical cue proteinmutation
24868377_3 6-12 ProteinMutation denotes 019S c rs34637584

PubMed_ArguminSci

Id Subject Object Predicate Lexical cue
T2 0-101 DRI_Background denotes The G2019S common mutation has been identified about 1% of sporadic cases and 4-7% of familial cases.