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Q37193903-39A41A1C-37F7-4136-B737-607EF93D1D47
Q37193903-39A41A1C-37F7-4136-B737-607EF93D1D47
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37193903-39A41A1C-37F7-4136-B737-607EF93D1D47
Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation.
P2860
Q37193903-39A41A1C-37F7-4136-B737-607EF93D1D47
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37193903-39A41A1C-37F7-4136-B737-607EF93D1D47
rank
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type
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Statement
wasDerivedFrom
1f31cc4bc6ace923112dd1aaff8b202fa626065e
P2860
Homozygous premature truncation of the HERG protein : the human HERG knockout.