1201 Whole Exon Deletion in the Claudin 16 Gene, a Novel Mutation in Familial Hypomagnesemia/Hypercalciuria/Nephrocalcinosis (FHHNC) and Sensorineural Deafness (SND)

Archives of Disease in Childhood - United Kingdom
doi 10.1136/archdischild-2012-302724.1201
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