A Dominant Mutation in Hexokinase 1 (HK1) Causes Retinitis Pigmentosa

Podobne zapisy

• Identification of a Novel Gene on 10q22.1 Causing Autosomal Dominant Retinitis Pigmentosa (adRP)
  od: Daiger, Stephen P., i wsp.
  Wydane: (2016)
• Molecular Findings in Families with an Initial Diagnose of Autosomal Dominant Retinitis Pigmentosa (adRP)
  od: Daiger, Stephen P., i wsp.
  Wydane: (2018)
• Polymorphic Variation of RPGRIP1L and IQCB1 as Modifiers of X-Linked Retinitis Pigmentosa Caused by Mutations in RPGR
  od: Fahim, Abigail T., i wsp.
  Wydane: (2012)
• Allelic Heterogeneity and Genetic Modifier Loci Contribute to Clinical Variation in Males with X-Linked Retinitis Pigmentosa Due to RPGR Mutations
  od: Fahim, Abigail T., i wsp.
  Wydane: (2011)
• North Carolina macular dystrophy (MCDR1) caused by a novel tandem duplication of the PRDM13 gene
  od: Bowne, Sara J., i wsp.
  Wydane: (2016)