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s10545-009-1108-x
s10545-009-1108-x
https://scigraph.springernature.com/pub.10.1007/s10545-009-1108-x
Comprehensive description of the phenotype of the first case of congenital disorder of glycosylation due to RFT1 deficiency (CDG In).
P2888
Q51780425-D9EA2E52-406D-4C4B-B02D-34E7A340975D
P2888
s10545-009-1108-x
https://scigraph.springernature.com/pub.10.1007/s10545-009-1108-x