Phexl222p mutation increases phex expression in a new enu mouse model for xlh disease

HIGHLIGHTS

• who: Carole El Hakam and collaborators from the (UNIVERSITY) have published the article: PHEXL222P Mutation Increases Phex Expression in a New ENU Mouse Model for XLH Disease, in the Journal: Genes 2022, 13, 1356. of /2022/
• what: PhexL222P mouse is a new ENU mouse model for XLH disease due to Leu to Pro amino_acid modification at position 222.

SUMMARY

HR could also be inherited in autosomal recessive form, namely ARHR1 (MIM 241520), caused by a mutation in the Dentin Matrix acidic Phosphoprotein 1 gene (DMP1); and ARHR2 (MIM 613312), caused by . . .

 



If you want to have access to all the content you need to log in!

Thanks :)

Username or E-mail:

If you don't have an account, you can create one here.