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Paper Details

Retinal Dysfunction in a Mouse Model of HCN1 Genetic Epilepsy.
1
2023
Ca, ERG abnormalities, HCN1, HCN1 Genetic Epilepsy, HCN1 channels, Hcn1, Hcn1 protein, M305L, Mouse, Retinal Dysfunction, attenuated, attenuated bipolar cell, catastrophic epilepsy, developmental and epileptic encephalopathy, epilepsy, epilepsy syndromes, genetic epilepsy, glutamate, human, mice, morphologic deficits, mouse, mutated HCN1, patient, patients, photoreceptors, retinal dysfunction, retinal ganglion cell, rod and cone photoreceptor inner segments, wild
Author NameAffiliation
Ingrid E SchefferFlorey Institute of Neuroscience and Mental Health
Ingrid E SchefferEpilepsy Research Centre, University of Melbourne/Austin Health
Ingrid E SchefferMurdoch Children's Research Institute, The Royal Children's Hospital
Ingrid E SchefferUniversity of Melbourne, Royal Children's Hospital
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Release 1.2