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Updated: Jan 7, 2026

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Distrofia retiniana asociada a IMPG2 con una nueva variante de error y opciones terapéuticas a través de la edición

Maram E A Abdalla Elsayed^1,2, Vincenzo Barone³, Maria Kaukonen⁴

¹Oxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.

Ophthalmic genetics

|January 1, 2026

Resumen

No abstract available in PubMed .

Palabras clave:

Edición de la base adenina Se incluyen los siguientes elementos:En el caso de las mujeres:distrofia hereditaria de la retina Distrofia de las barras y los conos

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