Identification of a New Mutation of the Myosin VII Head Region in Usher Syndrome Type 1

Hum Mutat. 1997;10(2):168-70. doi: 10.1002/(SICI)1098-1004(1997)10:2<168::AID-HUMU10>3.0.CO;2-Y.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Child
  • Diseases in Twins
  • Frameshift Mutation
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Male
  • Middle Aged
  • Mutation*
  • Myosins / genetics*
  • Nucleic Acid Heteroduplexes
  • Polymerase Chain Reaction
  • Polymorphism, Single-Stranded Conformational
  • Retinitis Pigmentosa / genetics*
  • Syndrome

Substances

  • Nucleic Acid Heteroduplexes
  • Myosins