Giri, D;
Bockenhauer, D;
Deshpande, C;
Achermann, JC;
Taylor, NF;
Rumsby, G;
Morgan, H;
... Ajzensztejn, M; + view all
(2020)
Co-Existence of Congenital Adrenal Hyperplasia and Bartter Syndrome due to Maternal Uniparental Isodisomy of HSD3B2 and CLCNKB Mutations.
Hormone Research in Paediatrics
10.1159/000507577.
(In press).