Novel AAV843 Vector-Mediated AGXT Gene Replacement Therapy Rescues the Primary Hyperoxaluria Type I Phenotype in Mice
收藏NIAID Data Ecosystem2026-05-02 收录
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https://www.ncbi.nlm.nih.gov/sra/SRP599819
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资源简介：
Primary hyperoxaluria type I (PH1) is an autosomal recessive disorder characterized by massive accumulations of oxalic acid resulting from abnormalities in the alanine-glyoxylate aminotransferase gene (AGXT).
创建时间：
2025-07-12
