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Q27683955-0800BD27-9D47-4F37-A526-24FB6469633C
Q27683955-0800BD27-9D47-4F37-A526-24FB6469633C
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http://www.wikidata.org/entity/statement/Q27683955-0800BD27-9D47-4F37-A526-24FB6469633C
Three rare diseases in one Sib pair: RAI1, PCK1, GRIN2B mutations associated with Smith–Magenis Syndrome, cytosolic PEPCK deficiency and NMDA receptor glutamate insensitivity
P2860
Q27683955-0800BD27-9D47-4F37-A526-24FB6469633C
BestRank
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http://www.wikidata.org/entity/statement/Q27683955-0800BD27-9D47-4F37-A526-24FB6469633C
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67bf2abef703c1ea3b2416a2ceadfabe6fd1a450
P2860
Thematic minireview series: a perspective on the biology of phosphoenolpyruvate carboxykinase 55 years after its discovery.