1. 1201 Whole Exon Deletion in the Claudin 16 Gene, a Novel Mutation in Familial Hypomagnesemia/Hypercalciuria/Nephrocalcinosis (FHHNC) and Sensorineural Deafness (SND). (October 2012) Authors: Sanjad, SA; Lu, Y; Khoury, C; Habbal, Z; Lifton, R Journal: Archives of disease in childhood Issue: Volume 97(2012)Supplement 2 Page Start: A343 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗