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Q44869368-18B0840C-9F6C-45CD-9797-ADFA7C70C0DD
Q44869368-18B0840C-9F6C-45CD-9797-ADFA7C70C0DD
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http://www.wikidata.org/entity/statement/Q44869368-18B0840C-9F6C-45CD-9797-ADFA7C70C0DD
Genetic and functional analyses describe a novel 730delG mutation in the KEL gene causing K0 phenotype in a Taiwanese blood donor.
P2860
Q44869368-18B0840C-9F6C-45CD-9797-ADFA7C70C0DD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44869368-18B0840C-9F6C-45CD-9797-ADFA7C70C0DD
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wasDerivedFrom
bbc577910ac8993f6804986c356b846da9d50b37
P2860
Heterozygosity for two novel null alleles of the KEL gene causes the Kell-null phenotype in a Japanese woman.