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Q33163304-AD9BF62B-7A26-4FA7-B704-6E6BE645D70B
Q33163304-AD9BF62B-7A26-4FA7-B704-6E6BE645D70B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33163304-AD9BF62B-7A26-4FA7-B704-6E6BE645D70B
Congenital long QT syndrome with compound mutations in the KCNH2 gene.
P2860
Q33163304-AD9BF62B-7A26-4FA7-B704-6E6BE645D70B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33163304-AD9BF62B-7A26-4FA7-B704-6E6BE645D70B
rank
NormalRank
type
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Statement
wasDerivedFrom
004ac8299b455117654bc7e29ef5da936162773a
P2860
Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation.