Biallelic RP1-associated retinal dystrophies: Expanding the mutational and clinical spectrum

PURPOSE: To evaluate the phenotypic spectrum of autosomal recessive RP1-associated retinal dystrophies and assess genotypic associations. METHODS: A retrospective multicenter study was performed of patients with biallelic RP1-associated retinal dystrophies. Data including presenting symptoms and age...

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Detalles Bibliográficos
Autores principales: Huckfeldt, Rachel M., Grigorian, Florin, Place, Emily, Comander, Jason I., Vavvas, Demetrios, Young, Lucy H., Yang, Paul, Shurygina, Maria, Pierce, Eric A., Pennesi, Mark E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7300197/
https://www.ncbi.nlm.nih.gov/pubmed/32565670

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7300197/
https://www.ncbi.nlm.nih.gov/pubmed/32565670

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