Delayed Diagnosis of Mild GLUT1 Deficiency Syndrome Caused by an Apparently De Novo SLC2A1 p.(Phe445del) Variant in a Child with a History of Severe Neonatal Hyperkalemia.
- DOI
- 10.3390/children13070883
- Published
- 2026 Jun 30
- Container
- Children (Basel, Switzerland)
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.3390/children13070883,
title = {Delayed Diagnosis of Mild GLUT1 Deficiency Syndrome Caused by an Apparently De Novo SLC2A1 p.(Phe445del) Variant in a Child with a History of Severe Neonatal Hyperkalemia.},
author = {Ivančan S and Debeljak M and Loboda T and Grosek Š},
year = {2026},
journal = {Children (Basel, Switzerland)},
doi = {10.3390/children13070883},
url = {https://doi.org/10.3390/children13070883}
}RIS
TY - JOUR TI - Delayed Diagnosis of Mild GLUT1 Deficiency Syndrome Caused by an Apparently De Novo SLC2A1 p.(Phe445del) Variant in a Child with a History of Severe Neonatal Hyperkalemia. AU - Ivančan S AU - Debeljak M AU - Loboda T AU - Grosek Š PY - 2026 JO - Children (Basel, Switzerland) DO - 10.3390/children13070883 UR - https://doi.org/10.3390/children13070883 ER -
APA
S, I., M, D., T, L., & Š, G. (2026). Delayed Diagnosis of Mild GLUT1 Deficiency Syndrome Caused by an Apparently De Novo SLC2A1 p.(Phe445del) Variant in a Child with a History of Severe Neonatal Hyperkalemia.. Children (Basel, Switzerland). https://doi.org/10.3390/children13070883
Source records
- pubmed · retrieved 2026-09-25T03:08:07.417Z