Barttin mutations in antenatal Bartter syndrome with sensorineural deafness

Pediatr Nephrol. 2006 Jul;21(7):1056-7. doi: 10.1007/s00467-006-0108-4. Epub 2006 May 24.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Bartter Syndrome / genetics*
  • Chloride Channels
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Infant, Newborn
  • Male
  • Membrane Proteins / genetics*
  • Mutation / genetics*

Substances

  • BSND protein, human
  • Chloride Channels
  • Membrane Proteins