1. A novel CASR mutation (p.Glu757Lys) causing autosomal dominant hypocalcaemia type 1. (1st October 2018) Authors: Kwan, Benjamin; Champion, Bernard; Boyages, Steven; Munns, Craig F; Clifton-Bligh, Roderick; Luxford, Catherine; Crawford, Bronwyn Journal: Endocrinology, diabetes & metabolism case reports Issue: (2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗