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Q24309032-AECBEBD2-E8C7-4F36-87D0-563F175FE0D5
Q24309032-AECBEBD2-E8C7-4F36-87D0-563F175FE0D5
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http://www.wikidata.org/entity/statement/Q24309032-AECBEBD2-E8C7-4F36-87D0-563F175FE0D5
Functional analysis of mutations in a severe congenital neutropenia syndrome caused by glucose-6-phosphatase-β deficiency
P2860
Q24309032-AECBEBD2-E8C7-4F36-87D0-563F175FE0D5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24309032-AECBEBD2-E8C7-4F36-87D0-563F175FE0D5
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wasDerivedFrom
114a8b2a1dff4f764f166a561355080c65f1744e
P2860
Phenotypic heterogeneity and evidence of a founder effect associated with G6PC3 mutations in patients with severe congenital neutropenia