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Paper Details

Development of therapies for rare genetic disorders of GPX4: roadmap and opportunities.
Orphanet J Rare Dis
11
2021
GPX4, GPX4-related diseases, GPx4, SSMD, Sedaghatian-type Spondylometaphyseal Dysplasia, genetic disorders, glutathione, glutathione peroxidase 4, patients, rare
Author NameAffiliation
Alysson R MuotriUniversity of California
Alysson R MuotriUniversity of California
Brent R StockwellColumbia University
Brent R StockwellColumbia University
Brent R StockwellColumbia University
Brent R StockwellColumbia University
Sanath Kumar Ramesh
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