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S10545-009-1108-X
S10545-009-1108-X
http://dx.doi.org/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).
P356
Q51780425-B804BF0E-3586-4DCA-BC93-58F289E161CB
P356
S10545-009-1108-X
http://dx.doi.org/10.1007/S10545-009-1108-X