Articles with "pex1 gly844asp" as a keyword



Photo by gavinbiesheuvel from unsplash

A longitudinal study of retinopathy in the PEX1-Gly844Asp mouse model for mild Zellweger Spectrum Disorder.

Sign Up to like & get
recommendations!
Published in 2019 at "Experimental eye research"

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