Defective EMC1 protein may contribute to a severe ocular disorder, familial exudative vitreoretinopathy

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In a recent study published in the journal Genes & Diseases, researchers from University of Electronic Science and Technology of China have uncovered a key relationship between the EMC1 protein and retinal vascular development. Mutations in the EMC1 gene appear to be associated with familial exudative vitreoretinopathy (FEVR), a severe ocular condition. The discovery offers potential new therapeutic avenues for treating this disorder and other related vascular defects.

retrieved 9 October 2023 from https://medicalxpress.com/news/2023-10-defective-emc1-protein-contribute-severe.html

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