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1 - 4 of 4 results found for IMPDH1.

  1. Retinitis pigmentosa: mutation analysis of RHO, PRPF31, RP1, and IMPDH1 genes in patients...

  2. Identification of Mutations in IMPDH1 in a Cohort of 96 Recessive RP Patients

  3. Sector Retinitis Pigmentosa: Extending the Molecular Genetics Basis and Elucidating the...

    PURPOSE: To determine the genetic background of sector retinitis pigmentosa (RP), natural history, in order to better inform patient counselling. DESIGN: Retrospective case series. METHODS: Review of clinical notes, retinal imaging including color

  4. Dominantly inherited retinal degeneration – exploring the spectrum of human retinal...

    The prevalence of retinal dystrophies among people with European ancestry is 1 in 3500-4000. Large majority of these conditions are caused by mutations in single genes inherited in autosomal recessive, autosomal dominant, X-linked recessive or

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