Advanced molecular approaches pave the road to a clear-cut diagnosis of hereditary retinal dystrophies

PURPOSE: The aim of this study was to identify the molecular genetic basis of hereditary retinal dystrophies (HRDs) in five unrelated Iranian families. METHODS: Whole exome sequencing and Sanger sequencing were performed in all families. Variants were analyzed using various bioinformatics databases...

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Detalles Bibliográficos
Autores principales: Ravesh, Zeinab, Dianatpour, Mahdi, Fardaei, Majid, Taghdiri, Maryam, Hashemi-Gorji, Feyzollah, Yassaee, Vahid Reza, Miryounesi, Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6197863/
https://www.ncbi.nlm.nih.gov/pubmed/30416334

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6197863/
https://www.ncbi.nlm.nih.gov/pubmed/30416334

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