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Q51748265-42DBE6D0-67A0-41CB-90DA-79C170EC54F4
Q51748265-42DBE6D0-67A0-41CB-90DA-79C170EC54F4
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http://www.wikidata.org/entity/statement/Q51748265-42DBE6D0-67A0-41CB-90DA-79C170EC54F4
Cellular mechanisms underlying the increased disease severity seen for patients with long QT syndrome caused by compound mutations in KCNQ1.
P2860
Q51748265-42DBE6D0-67A0-41CB-90DA-79C170EC54F4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51748265-42DBE6D0-67A0-41CB-90DA-79C170EC54F4
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wasDerivedFrom
d1642ebbbba08bf44c071bcc39e8e617e0b2ff4d
P2860
The N-terminal juxtamembranous domain of KCNQ1 is critical for channel surface expression: implications in the Romano-Ward LQT1 syndrome.