PHEX<sup>L222P</sup> Mutation Increases <i>Phex</i> Expression in a New ENU Mouse Model for XLH Disease
<i>Phex<sup>L222P</sup></i> mouse is a new ENU mouse model for XLH disease due to Leu to Pro amino acid modification at position 222. <i>Phex<sup>L222P</sup></i> mouse is characterized by growth retardation, hypophosphatemia, hypocalcemia, reduced body...
| Main Authors: | , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2022-07-01
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| Series: | Genes |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2073-4425/13/8/1356 |