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Q37101121-3DA9954F-5656-4F2D-AD0A-96172F302D0A
Q37101121-3DA9954F-5656-4F2D-AD0A-96172F302D0A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37101121-3DA9954F-5656-4F2D-AD0A-96172F302D0A
HAX1 deletion impairs BCR internalization and leads to delayed BCR-mediated apoptosis.
P2860
Q37101121-3DA9954F-5656-4F2D-AD0A-96172F302D0A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37101121-3DA9954F-5656-4F2D-AD0A-96172F302D0A
rank
NormalRank
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Statement
wasDerivedFrom
fc597e2eef1c0b9645aac084a38b028b12953c97
P2860
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)