Associated Papers
X-linked transient antenatal Bartter syndrome related to MAGED2 gene: Enriching the phenotypic description and pathophysiologic investigation.
Buffet A et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2025
A Case Report and Literature Review of a Novel Mutation in the MAGED2 Gene of a Patient With Severe Transient Polyhydramnios.
Wu X et al.
Frontiers in Pediatrics, 2021
A step towards precision medicine in management of severe transient polyhydramnios: MAGED2 variant.
Arthuis CJ et al.
Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology, 2019
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