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Q28273669-C8E37C6C-BCBD-4152-A41B-BAAC75421E56
Q28273669-C8E37C6C-BCBD-4152-A41B-BAAC75421E56
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28273669-C8E37C6C-BCBD-4152-A41B-BAAC75421E56
Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update)
P2860
Q28273669-C8E37C6C-BCBD-4152-A41B-BAAC75421E56
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28273669-C8E37C6C-BCBD-4152-A41B-BAAC75421E56
rank
NormalRank
type
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Statement
wasDerivedFrom
729ac6dd962f899489351c9cdf138154247ae4a1
P2860
A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous disease