Correction: Exome Sequencing of Index Patients with Retinal Dystrophies as a Tool for Molecular Diagnosis

Samankaltaisia teoksia

• Exome Sequencing of Index Patients with Retinal Dystrophies as a Tool for Molecular Diagnosis
  Tekijä: Corton, Marta, et al.
  Julkaistu: (2013)
• High frequency of CRB1 mutations as cause of Early-Onset Retinal Dystrophies in the Spanish population
  Tekijä: Corton, Marta, et al.
  Julkaistu: (2013)
• Identification of two novel mutations in CDHR1 in consanguineous Spanish families with autosomal recessive retinal dystrophy
  Tekijä: Nikopoulos, Konstantinos, et al.
  Julkaistu: (2015)
• Homozygosity mapping reveals novel and known mutations in Pakistani families with inherited retinal dystrophies
  Tekijä: Saqib, Muhammad Arif Nadeem, et al.
  Julkaistu: (2015)
• Outcome of ABCA4 disease-associated alleles in autosomal recessive Retinal Dystrophies: Retrospective analysis in 420 Spanish families
  Tekijä: Riveiro-Alvarez, Rosa, et al.
  Julkaistu: (2013)