De novo mutation in ATP6V1B2 impairs lysosome acidification and causes dominant deafness-onychodystrophy syndrome

Cell Res. 2014 Nov;24(11):1370-3. doi: 10.1038/cr.2014.77. Epub 2014 Jun 10.
No abstract available

Publication types

  • Letter
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Cell Line
  • Cochlea / metabolism
  • Cochlea / pathology
  • Female
  • Hearing Loss / congenital
  • Hearing Loss / genetics*
  • Hearing Loss / pathology
  • Heterozygote
  • Humans
  • Lysosomes / metabolism
  • Male
  • Mice
  • Molecular Sequence Data
  • Morpholinos / metabolism
  • Nail Diseases / congenital
  • Nail Diseases / genetics*
  • Nail Diseases / pathology
  • Pedigree
  • Phenotype
  • Polymorphism, Single Nucleotide
  • Sequence Alignment
  • Sequence Analysis, DNA
  • Vacuolar Proton-Translocating ATPases / antagonists & inhibitors
  • Vacuolar Proton-Translocating ATPases / genetics*
  • Vacuolar Proton-Translocating ATPases / metabolism

Substances

  • Morpholinos
  • Vacuolar Proton-Translocating ATPases
  • ATP6V1B2 protein, human