A novel mutation in the PRPH2 gene in a Chinese pedigree with retinitis pigmentosa and angle-closure glaucoma

BACKGROUND: Retinitis pigmentosa (RP) is a rare, progressive, and hereditary disorder that leads to the progressive loss of vision and visual field, and in some cases blindness. The specific relationship between RP and glaucoma has been debated for decades. METHODS: In this study, we examined a Han...

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Detalles Bibliográficos
Autores principales: Li, Wei-ning, Du, Xiu-juan, Zhang, Yu-ting, Wang, Le-yi, Zhu, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8369728/
https://www.ncbi.nlm.nih.gov/pubmed/34399712
http://dx.doi.org/10.1186/s12886-021-02064-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8369728/
https://www.ncbi.nlm.nih.gov/pubmed/34399712
http://dx.doi.org/10.1186/s12886-021-02064-5

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