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Q33830119-7082EA3A-13C5-4A84-BD8A-9E315220EE26
Q33830119-7082EA3A-13C5-4A84-BD8A-9E315220EE26
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33830119-7082EA3A-13C5-4A84-BD8A-9E315220EE26
The syndrome of inherited partial SBP2 deficiency in humans.
P2860
Q33830119-7082EA3A-13C5-4A84-BD8A-9E315220EE26
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33830119-7082EA3A-13C5-4A84-BD8A-9E315220EE26
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Statement
wasDerivedFrom
d290bf690dae6eeadb7fdfc5efb04e19027786d3
P2860
Clinical and molecular characterization of a novel selenocysteine insertion sequence-binding protein 2 (SBP2) gene mutation (R128X).