Peroxin-7 is a receptor associated with Refsum's disease and rhizomelic chondrodysplasia punctata type 1. Peroxin-7 is encoded in humans by the PEX7 gene.
See also Peroxin
References
External links GeneReviews/NCBI/NIH/UW entry on Refsum Disease GeneReviews/NIH/NCBI/UW entry on Rhizomelic Chondrodysplasia Punctata Type 1 PEX7+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)