A longitudinal study of retinopathy in the PEX1-Gly844Asp mouse model for mild Zellweger Spectrum Disorder.
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DOI: 10.1016/j.exer.2019.107713
Abstract: Zellweger Spectrum Disorder (ZSD) is an autosomal recessive disease caused by mutations in any one of 13 PEX genes whose protein products are required for peroxisome assembly. Retinopathy leading to blindness is one of the… read more here.
Keywords: zellweger spectrum; pex1 gly844asp; spectrum disorder; pex1 ... See more keywords