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Q43936473-10D3F5DF-F6BE-46DF-9809-C58B535C6B6E
Q43936473-10D3F5DF-F6BE-46DF-9809-C58B535C6B6E
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Statement
http://www.wikidata.org/entity/statement/Q43936473-10D3F5DF-F6BE-46DF-9809-C58B535C6B6E
Heterozygosity for two novel null alleles of the KEL gene causes the Kell-null phenotype in a Japanese woman.
P2860
Q43936473-10D3F5DF-F6BE-46DF-9809-C58B535C6B6E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43936473-10D3F5DF-F6BE-46DF-9809-C58B535C6B6E
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type
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Statement
wasDerivedFrom
5c00cb7af9903393a15fe2badd7de44b8d1f7781
P2860
Association of XK and Kell blood group proteins