DOI:
10.1055/s-00034916
Nervenheilkunde
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References
Dorre K, Olczak M, Wada Y. et al
A new case of UDP-galactose transporter deficiency (SLC35A2-CDG): molecular basis, clinical phenotype, and therapeutic approach.
Journal of inherited metabolic disease 2015;
38 (05) 931-940
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