新型BEST1变异与两位兄弟姐妹的非典型白状黄斑变异相关:表型和遗传特征

Beatriz De-Pablo-Gómez-De-Liaño1, Laura Moralejo-Vázquez1, Carlos Llorente-La-Orden1

  • 1Department of Ophthalmology, Hospital Central de la Cruz Roja San José y Santa Adela, Madrid, Spain.

Ophthalmic genetics
|March 11, 2026
PubMed
概括

一种新的BEST1基因变异在两个兄弟姐妹中引起了小状黄斑变异. 这一发现扩大了已知的贝斯特罗菲诺病的遗传原因,贝斯特罗菲诺病是一组遗传性视网膜疾病.

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