De novo HNF1 homeobox B mutation as a cause for chronic, treatment-resistant hypomagnesaemia

Bockenhauer, D; Stiles, CE; Thursaisingham, R; Platts, L; Kumar, A; Korbonits, M; (2018) De novo HNF1 homeobox B mutation as a cause for chronic, treatment-resistant hypomagnesaemia. Endocrinology, Diabetes and Metabolism Case Reports (In press).

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