Dorotea Ninković
2PUBLICATIONS
1CO-AUTHORS
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Publications (2)
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|Sep 23, 2018
Hypogammaglobulinemia and imaging features in a patient with infantile free sialic acid storage disease (ISSD) and a novel mutation in the SLC17A5 gene.Tamara Žigman, Danijela Petković Ramadža, Mario Lušić
|Jul 08, 2016
Hyperinsulinism-hyperammonemia syndrome: a de novo mutation of the GLUD1 gene in twins and a review of the literature.Dorotea Ninković, Vladimir Sarnavka, Anica Bašnec
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