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Q51780425-F5684C4C-6F3B-407C-89F6-0A605A5C1F26
Q51780425-F5684C4C-6F3B-407C-89F6-0A605A5C1F26
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51780425-F5684C4C-6F3B-407C-89F6-0A605A5C1F26
Comprehensive description of the phenotype of the first case of congenital disorder of glycosylation due to RFT1 deficiency (CDG In).
P2860
Q51780425-F5684C4C-6F3B-407C-89F6-0A605A5C1F26
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51780425-F5684C4C-6F3B-407C-89F6-0A605A5C1F26
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wasDerivedFrom
0be0935326988090ed259010a9a36df6a29f15ec
P2860
Human RFT1 deficiency leads to a disorder of N-linked glycosylation