ArticleFrontiers in neuroscience2026
Mouse model of Angelman syndrome exhibits reduced retinal activity during development.
Article in Frontiers in neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Angelman Syndrome (AS) is a neurodevelopmental disorder characterized by intellectual disability, seizures, and motor dysfunction caused by loss of function of the maternal UBE3A allele. A large proportion of patients exhibit visual impairments, but the underlying circuit-level mechanisms are not well understood. Spontaneous retinal waves provide essential patterned activity that guides the wiring and refinement of retinofugal projections to visual brain centers during a critical early developmental window. Here, using high-density microelectrode array recordings from postnatal day 8-11 mouse retinas, we demonstrate that
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