Mini-PCDH15 gene therapy rescues hearing in a mouse model of Usher syndrome type 1F

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Last updated 07 juin 2024

USH1F Current Research : USH Gene-Specific Research : Research : Usher Syndrome Coalition

Proposed therapy, developed in a Pcdh15-deficient mouse, for progressive loss of vision in human Usher syndrome

PDF) Proposed therapy, developed in a Pcdh15-deficient mouse, for progressive loss of vision in human Usher Syndrome

Mini-PCDH15 gene therapy rescues hearing in a mouse model of Usher syndrome type 1F

The genetic and phenotypic landscapes of Usher syndrome: from disease mechanisms to a new classification

Rescue of hearing by adenine base editing in a humanized mouse model of Usher syndrome type 1F: Molecular Therapy

Proposed therapy, developed in a Pcdh15-deficient mouse, for progressive loss of vision in human Usher syndrome

USH1F Current Research : USH Gene-Specific Research : Research : Usher Syndrome Coalition

Dual AAV-based PCDH15 gene therapy achieves sustained rescue of visual function in a mouse model of Usher syndrome 1F - ScienceDirect

PCDH15 Dual-AAV Gene Therapy for Deafness and Blindness in Usher Syndrome Type 1F

Mini-PCDH15 gene therapy rescues hearing in a mouse model of Usher syndrome type 1F

Usher Syndrome, Type if disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials

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