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Q51780425-1DE03BFF-A636-4CC1-9B6B-EC4CA0D75349
Q51780425-1DE03BFF-A636-4CC1-9B6B-EC4CA0D75349
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Statement
http://www.wikidata.org/entity/statement/Q51780425-1DE03BFF-A636-4CC1-9B6B-EC4CA0D75349
Comprehensive description of the phenotype of the first case of congenital disorder of glycosylation due to RFT1 deficiency (CDG In).
P2860
Q51780425-1DE03BFF-A636-4CC1-9B6B-EC4CA0D75349
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51780425-1DE03BFF-A636-4CC1-9B6B-EC4CA0D75349
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wasDerivedFrom
0be0935326988090ed259010a9a36df6a29f15ec
P2860
Congenital disorders of glycosylation: genetic model systems lead the way.