Mutations in the X-Linked Retinitis Pigmentosa Genes RPGR and RP2 Found in 8.5% of Families with a Provisional Diagnosis of Autosomal Dominant Retinitis Pigmentosa

مواد مشابهة

• Molecular Findings in Families with an Initial Diagnose of Autosomal Dominant Retinitis Pigmentosa (adRP)
  بواسطة: Daiger, Stephen P., وآخرون
  منشور في: (2018)
• MUTATIONS IN KNOWN GENES ACCOUNT FOR 58% OF AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA (adRP)
  بواسطة: Daiger, Stephen P., وآخرون
  منشور في: (2008)
• Mutations in the TOPORS gene cause 1% of autosomal dominant retinitis pigmentosa
  بواسطة: Bowne, Sara J., وآخرون
  منشور في: (2008)
• Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa
  بواسطة: Bowne, Sara J., وآخرون
  منشور في: (2002)
• Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosa
  بواسطة: Bowne, Sara J., وآخرون
  منشور في: (1999)