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Q36925245-75624C1D-1198-4685-B156-F596F7ED5F43
Q36925245-75624C1D-1198-4685-B156-F596F7ED5F43
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36925245-75624C1D-1198-4685-B156-F596F7ED5F43
Congenital protein hypoglycosylation diseases.
P2860
Q36925245-75624C1D-1198-4685-B156-F596F7ED5F43
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36925245-75624C1D-1198-4685-B156-F596F7ED5F43
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wasDerivedFrom
6d3e09ffbb5144a5fbc11d1a17eccfa6406fde83
P2860
Comprehensive description of the phenotype of the first case of congenital disorder of glycosylation due to RFT1 deficiency (CDG In).