Corrigendum: Panel-based NGS Reveals Novel Pathogenic Mutations in Autosomal Recessive Retinitis Pigmentosa

Ejemplares similares

• Panel-based NGS Reveals Novel Pathogenic Mutations in Autosomal Recessive Retinitis Pigmentosa
  por: Perez-Carro, Raquel, et al.
  Publicado: (2016)
• Identification of the Photoreceptor Transcriptional Co-Repressor SAMD11 as Novel Cause of Autosomal Recessive Retinitis Pigmentosa
  por: Corton, M., et al.
  Publicado: (2016)
• Mutation analysis of 272 Spanish families affected by autosomal recessive retinitis pigmentosa using a genotyping microarray
  por: Ávila-Fernández, Almudena, et al.
  Publicado: (2010)
• Genotyping microarray: Mutation screening in Spanish families with autosomal dominant retinitis pigmentosa
  por: Blanco-Kelly, Fiona, et al.
  Publicado: (2012)
• Identification of two novel mutations in CDHR1 in consanguineous Spanish families with autosomal recessive retinal dystrophy
  por: Nikopoulos, Konstantinos, et al.
  Publicado: (2015)