Spectrum of phenotypic findings in individuals with Joubert syndrome and clinical correlation with identified mutations in the NPHP1,AHI1, and RPGRIP1L genes

Parisi M. A., Doherty D., Arts H. H., Gorden N. T., Eckert M. L., Shaw D. W. W., ...More

132nd Annual Meeting of the American-Neurological-Association, Washington, Kiribati, 7 - 10 October 2007, vol.62, pp.537-538 identifier

  • Publication Type: Conference Paper / Summary Text
  • Volume: 62
  • City: Washington
  • Country: Kiribati
  • Page Numbers: pp.537-538
  • Dokuz Eylül University Affiliated: No