DOI: 10.1055/s-00034916

Nervenheilkunde

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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