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Article

Barttin mutations in antenatal Bartter syndrome with sensorineural deafness.

Pediatric nephrology (Berlin, Germany) - 1 Jul 2006

Ozlu Ferda, Yapicioğlu Hacer, Satar Mehmet, Narli Nejat, Ozcan Kenan, Buyukcelik Mithat, Konrad Martin, Demirhan Osman

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Share to Bartter Syndrome
Share to Chloride Channels
Share to Hearing Loss, Sensorineural
Share to Infant, Newborn

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Membrane Proteins

Share to Mutation

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Identifiers

PMID: 16773427
DOI: 10.1007/s00467-006-0108-4

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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