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Q43668587-3BBD44B4-CA3E-4B25-8B48-D354513782F6
Q43668587-3BBD44B4-CA3E-4B25-8B48-D354513782F6
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Statement
http://www.wikidata.org/entity/statement/Q43668587-3BBD44B4-CA3E-4B25-8B48-D354513782F6
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
Q43668587-3BBD44B4-CA3E-4B25-8B48-D354513782F6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43668587-3BBD44B4-CA3E-4B25-8B48-D354513782F6
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0cf188f263822ce9c018e4a0fc2fcf7ae34cc0ce
P2860
Genetics and clinical destiny: improving care in hypertrophic cardiomyopathy