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