A Novel Conserved Cochlear Gene, OTOR: Identification, Expression Analysis, and Chromosomal Mapping

This publication has 35 references indexed in Scilit:

• High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene.
  Human Molecular Genetics, 1999
• A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects
  Human Molecular Genetics, 1999
• Otogelin: A glycoprotein specific to the acellular membranes of the inner ear
  Proceedings of the National Academy of Sciences, 1997
• Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
  Nucleic Acids Research, 1997
• Cloning of the Genes Encoding Two Murine and Human Cochlear Unconventional Type I Myosins
  Genomics, 1997
• Cloning of a Retinoic Acid-sensitive mRNA Expressed in Cartilage and during Chondrogenesis
  Published by Elsevier ,1996
• Alagille syndrome and deletion of 20p.
  Journal of Medical Genetics, 1990
• A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
  Analytical Biochemistry, 1984
• A comprehensive set of sequence analysis programs for the VAX
  Nucleic Acids Research, 1984
• Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease
  Biochemistry, 1979