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Q37147381-2C192E87-4C7C-461D-8FC4-94CA545426A2
Q37147381-2C192E87-4C7C-461D-8FC4-94CA545426A2
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Statement
http://www.wikidata.org/entity/statement/Q37147381-2C192E87-4C7C-461D-8FC4-94CA545426A2
Single nucleotide deletion mutation of KCNH2 gene is responsible for LQT syndrome in a 3-generation Korean family.
P2860
Q37147381-2C192E87-4C7C-461D-8FC4-94CA545426A2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37147381-2C192E87-4C7C-461D-8FC4-94CA545426A2
rank
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type
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Statement
wasDerivedFrom
cad5fb69eaa8b0236d034710c66f9fd8413c11a0
P2860
The human delta1261 mutation of the HERG potassium channel results in a truncated protein that contains a subunit interaction domain and decreases the channel expression