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Q51748265-1C80D2FF-B5DC-4D12-AF78-FB2109F5FD83
Q51748265-1C80D2FF-B5DC-4D12-AF78-FB2109F5FD83
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http://www.wikidata.org/entity/statement/Q51748265-1C80D2FF-B5DC-4D12-AF78-FB2109F5FD83
Cellular mechanisms underlying the increased disease severity seen for patients with long QT syndrome caused by compound mutations in KCNQ1.
P2860
Q51748265-1C80D2FF-B5DC-4D12-AF78-FB2109F5FD83
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51748265-1C80D2FF-B5DC-4D12-AF78-FB2109F5FD83
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wasDerivedFrom
d1642ebbbba08bf44c071bcc39e8e617e0b2ff4d
P2860
Prevalence and potential genetic determinants of sensorineural deafness in KCNQ1 homozygosity and compound heterozygosity