BEST1 mutation correction
收藏NIAID Data Ecosystem2026-05-02 收录
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资源简介：
In this study, we identified a homozygous deep intron variation (DIV), c.867+97G>A, in a case of ARB that exhibits atypical clinical features. Furthermore, ABE was harnessed for the targeted gene correction.
创建时间：
2025-03-22
