Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophy
2025 · Genetics in Medicine · 3 citations
https://doi.org/10.1016/j.gim.2025.101401
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Maayan Avraham
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Maayan Avraham is an academic researcher.
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