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Q33807877-AF19C083-E25E-4492-8E2D-90DEFDFC2C11
Q33807877-AF19C083-E25E-4492-8E2D-90DEFDFC2C11
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Statement
http://www.wikidata.org/entity/statement/Q33807877-AF19C083-E25E-4492-8E2D-90DEFDFC2C11
Familial hypertrophic cardiomyopathy owing to double heterozygosity for a 403Arg--> Trp mutation in exon 13 of the MYH7 gene and a novel mutation, 453Arg--> His, in exon 14 of the MYH7 gene: A case report.
P2860
Q33807877-AF19C083-E25E-4492-8E2D-90DEFDFC2C11
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33807877-AF19C083-E25E-4492-8E2D-90DEFDFC2C11
rank
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type
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Statement
wasDerivedFrom
aa577d7461bf06c220091176def671d6e9441f15
P2860
Hypertrophic cardiomyopathy: evaluation and treatment of patients at high risk for sudden death.