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Q45897769-B73CA19F-C778-4734-A134-9295BC228932
Q45897769-B73CA19F-C778-4734-A134-9295BC228932
BestRank
Statement
http://www.wikidata.org/entity/statement/Q45897769-B73CA19F-C778-4734-A134-9295BC228932
Molecular study of congenital erythrocytosis in 70 unrelated patients revealed a potential causal mutation in less than half of the cases (Where is/are the missing gene(s)?).
P2860
Q45897769-B73CA19F-C778-4734-A134-9295BC228932
BestRank
Statement
http://www.wikidata.org/entity/statement/Q45897769-B73CA19F-C778-4734-A134-9295BC228932
rank
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type
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Statement
wasDerivedFrom
485dde551849eb335d6842de34ffe49f333b19a5
P2860
Isolated erythrocytosis: study of 67 patients and identification of three novel germ-line mutations in the prolyl hydroxylase domain protein 2 (PHD2) gene.