Article info
PDFCase Reports: Rare disease
HNF1B variant without hyperglycaemia as a cause of isolated profound hypomagnesaemia
- Correspondence to Dr Shobitha Vollmer; Shobitha.Vollmer{at}skane.se
Citation
HNF1B variant without hyperglycaemia as a cause of isolated profound hypomagnesaemia
Publication history
- Accepted February 1, 2023
- First published February 9, 2023.
Online issue publication
February 09, 2023
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
© BMJ Publishing Group Limited 2023. No commercial re-use. See rights and permissions. Published by BMJ.