Increasing evidence for syndromic phenotypes associated with RPGR mutations

Am J Ophthalmol. 2004 Apr;137(4):785-6; author reply 786. doi: 10.1016/j.ajo.2003.11.050.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Eye Proteins / genetics*
  • Frameshift Mutation*
  • Genetic Diseases, X-Linked / genetics*
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Phenotype
  • Retinitis Pigmentosa / genetics*
  • Syndrome

Substances

  • Eye Proteins
  • RPGR protein, human