Identification of a Novel Gene on 10q22.1 Causing Autosomal Dominant Retinitis Pigmentosa (adRP)

Παρόμοια τεκμήρια

• Molecular Findings in Families with an Initial Diagnose of Autosomal Dominant Retinitis Pigmentosa (adRP)
  ανά: Daiger, Stephen P., κ.ά.
  Έκδοση: (2018)
• Identification of Disease-Causing Mutations in Autosomal Dominant Retinitis Pigmentosa (adRP) Using Next-Generation DNA Sequencing
  ανά: Bowne, Sara J., κ.ά.
  Έκδοση: (2011)
• Application of Next-Generation Sequencing to Identify Genes and Mutations Causing Autosomal Dominant Retinitis Pigmentosa (adRP)
  ανά: Daiger, Stephen P., κ.ά.
  Έκδοση: (2014)
• MUTATIONS IN KNOWN GENES ACCOUNT FOR 58% OF AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA (adRP)
  ανά: Daiger, Stephen P., κ.ά.
  Έκδοση: (2008)
• Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa
  ανά: Bowne, Sara J., κ.ά.
  Έκδοση: (2002)