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Clinical and whole exome sequencing findings in children from Yunnan Yi minority ethnic group with retinitis pigmentosa: two case reports
BACKGROUND: Retinitis pigmentosa is a group of rare hereditary retinal dystrophy diseases that lead to difficulty seeing at night, progressive loss of peripheral field vision (tunnel vision), and eventual loss of central vision. However, a genetic cause cannot be determined in approximately 60% of c...
Autores principales: | Xiao, Yi-shuang, He, Wen-Ji, Jiang, Hong-chao, Tan, Li, Ma, Jing, Zhang, Zhen |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10236786/ https://www.ncbi.nlm.nih.gov/pubmed/37264419 http://dx.doi.org/10.1186/s13256-023-03830-3 |
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