Segregation of a PRKCG mutation in two RP11 families.

Podobne zapisy

• RP11 is the second most common locus for dominant retinitis pigmentosa.
  od: Vithana, E, i wsp.
  Wydane: (1998)
• Evidence for a major retinitis pigmentosa locus on 19q13.4 (RP11) and association with a unique bimodal expressivity phenotype.
  od: Al-Maghtheh, M., i wsp.
  Wydane: (1996)
• No mutations in the coding region of the PRKCG gene in three families with retinitis pigmentosa linked to the RP11 locus on chromosome 19q.
  od: Dryja, T P, i wsp.
  Wydane: (1999)
• A new dominant retinitis pigmentosa family mapping to the RP18 locus on chromosome 1q11-21.
  od: Inglehearn, C F, i wsp.
  Wydane: (1998)
• A linkage survey of 20 dominant retinitis pigmentosa families: frequencies of the nine known loci and evidence for further heterogeneity.
  od: Inglehearn, C F, i wsp.
  Wydane: (1998)