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Q48193679-E2BA3F34-010D-44C3-BD5D-D0966F84BA02
Q48193679-E2BA3F34-010D-44C3-BD5D-D0966F84BA02
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48193679-E2BA3F34-010D-44C3-BD5D-D0966F84BA02
Identification of a novel B allele with a missense mutation (c.721C>G) in a Korean family with a weak B phenotype.
P2860
Q48193679-E2BA3F34-010D-44C3-BD5D-D0966F84BA02
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48193679-E2BA3F34-010D-44C3-BD5D-D0966F84BA02
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
fca4656da44a8e9fdf4cdb383f910805d9de633e
P2860
Weak A phenotypes associated with novel ABO alleles carrying the A2-related 1061C deletion and various missense substitutions.