PMC:1852721 / 57480-57884 JSONTXT

{"project":"2_test","denotations":[{"id":"17357067-15044642-2054081","span":{"begin":218,"end":220},"obj":"15044642"}],"text":"Bartter syndrome type 4 (MIM #602522)—renal salt wasting and deafness—is most often caused by mutation in the BSND gene (MIM *606412). In a child with this disorder whose parents were consanguineous, Schlingmann et al.67 found no mutation in the BSND gene but found homozygous deletion of the CLCNKB gene (MIM *602023.0008) and a homozygous missense mutation of the linked CLCNKA gene (MIM *602024.0001)."}