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PEDS.2011-2711
PEDS.2011-2711
http://dx.doi.org/10.1542/PEDS.2011-2711
Defining the phenotype in congenital disorder of glycosylation due to ALG1 mutations.
P356
Q41933339-F58810C1-CEEF-40E5-96FF-940F06692E44
P356
PEDS.2011-2711
http://dx.doi.org/10.1542/PEDS.2011-2711