Expression pattern of the mouse ortholog of the Pendred’s syndrome gene (Pds) suggests a key role for pendrin in the inner ear

Gelijkaardige items

• Localization and Functional Studies of Pendrin in the Mouse Inner Ear Provide Insight About the Etiology of Deafness in Pendred Syndrome
  door: Royaux, Ines E., et al.
  Gepubliceerd in: (2003)
• Development of the Mouse Inner Ear and Origin of Its Sensory Organs
  door: Morsli, Hakim, et al.
  Gepubliceerd in: (1998)
• The Role of Pendrin in the Development of the Murine Inner Ear
  door: Wangemann, Philine
  Gepubliceerd in: (2011)
• Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome
  door: Coucke, P, et al.
  Gepubliceerd in: (1999)
• Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion
  door: Royaux, Ines E., et al.
  Gepubliceerd in: (2001)