We have carried out a mutation screening of the PHEX gene in Finnish patients with hypophosphatemia. A total of 100% (5/5) of the familial HYP patients (X-linked hypophosphatemia) and 93% (14/15) of the sporadic cases were found to carry a mutation in the PHEX gene. We identified 18 mutations, of wh
✦ LIBER ✦
Periapical and endodontic status of permanent teeth in patients with hypophosphatemic rickets
✍ Scribed by M. G. ANDERSEN; S. S. BECK-NIELSEN; D. HAUBEK; H. HINTZE; H. GJØRUP; S. POULSEN
- Book ID
- 108882118
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 189 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0305-182X
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