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

مواد مشابهة

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