Mutations in ARL2BP, Encoding ADP-Ribosylation-Factor-Like 2 Binding Protein, Cause Autosomal-Recessive Retinitis Pigmentosa

Samankaltaisia teoksia

• Nonsyndromic retinitis pigmentosa is highly prevalent in the Jerusalem region with a high frequency of founder mutations
  Tekijä: Sharon, Dror, et al.
  Julkaistu: (2015)
• Exome sequencing identifies a founder frameshift mutation in an alternative exon of USH1C as the cause of autosomal recessive retinitis pigmentosa with late-onset hearing loss.
  Tekijä: Samer Khateb, et al.
  Julkaistu: (2012-01-01)
• Exome Sequencing Identifies a Founder Frameshift Mutation in an Alternative Exon of USH1C as the Cause of Autosomal Recessive Retinitis Pigmentosa with Late-Onset Hearing Loss
  Tekijä: Khateb, Samer, et al.
  Julkaistu: (2012)
• Novel homozygous splicing mutations in ARL2BP cause autosomal recessive retinitis pigmentosa
  Tekijä: Fiorentino, Alessia, et al.
  Julkaistu: (2018)
• ADP Ribosylation Factor Like 2 (Arl2) Regulates Breast Tumor Aggressivity in Immunodeficient Mice
  Tekijä: Beghin, Anne, et al.
  Julkaistu: (2009)