Two novel mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene in X-linked retinitis pigmentosa (RP3). Mutations in brief no. 172. Online

Hum Mutat. 1998;12(3):212-3.

Abstract

Recently a new gene called RPGR (retinitis pigmentosa GTPase regulator) was isolated in Xp21.1 and found to be mutated in patients with RP3 type X-linked retinitis pigmentosa. Two new mutations, the first a single base pair deletion and the other a two base pairs deletion, have been found in one Spanish and one Italian family.

MeSH terms

  • Carrier Proteins / genetics*
  • Dyneins / genetics
  • Genetic Linkage
  • Humans
  • Mutation / genetics*
  • Proteins / genetics*
  • Retinitis Pigmentosa / genetics*
  • Sequence Deletion
  • X Chromosome / genetics*

Substances

  • Carrier Proteins
  • Proteins
  • Dyneins