Szymańska, E., Rokicki, D., Wątrobinska, U., Ciara, E., Halat, P., Płoski, R., & Tylki-Szymańka, A. (2015). Pediatric patient with hyperketotic hypoglycemia diagnosed with glycogen synthase deficiency due to the novel homozygous mutation in GYS2. Mol Genet Metab Rep.

Szymańska, Edyta, Dariusz Rokicki, Urszula Wątrobinska, Elżbieta Ciara, Paulina Halat, Rafał Płoski, and Anna Tylki-Szymańka. "Pediatric Patient With Hyperketotic Hypoglycemia Diagnosed With Glycogen Synthase Deficiency Due to the Novel Homozygous Mutation in GYS2." Mol Genet Metab Rep 2015.

Szymańska, Edyta, et al. "Pediatric Patient With Hyperketotic Hypoglycemia Diagnosed With Glycogen Synthase Deficiency Due to the Novel Homozygous Mutation in GYS2." Mol Genet Metab Rep 2015.