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Q43668587-29D2FFCD-F1D0-42D8-8089-002E6D4A8738
Q43668587-29D2FFCD-F1D0-42D8-8089-002E6D4A8738
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Statement
http://www.wikidata.org/entity/statement/Q43668587-29D2FFCD-F1D0-42D8-8089-002E6D4A8738
Two founder mutations in the alpha-tropomyosin and the cardiac myosin-binding protein C genes are common causes of hypertrophic cardiomyopathy in the Finnish population.
P2860
Q43668587-29D2FFCD-F1D0-42D8-8089-002E6D4A8738
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43668587-29D2FFCD-F1D0-42D8-8089-002E6D4A8738
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type
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0cf188f263822ce9c018e4a0fc2fcf7ae34cc0ce
P2860
Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands