Novel PHEX gene locus-specific database
What is PHEX Gene Hypophosphatemic rickets, X-linked NGS Genetic DNA Test ?
FGF23 and its role in X-linked hypophosphatemia-related morbidity | Orphanet Journal of Rare Diseases | Full Text
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XLH Overview | For HCPs
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PHEX gene and hypophosphatemia - ScienceDirect
Schematic representation of the PHEX gene with the localization of the... | Download Scientific Diagram
FGF23 and its role in X-linked hypophosphatemia-related morbidity | Orphanet Journal of Rare Diseases | Full Text
PHEX Gene - GeneCards | PHEX Protein | PHEX Antibody
CASE REPORT MOLECULAR ANALYSIS CONCLUSION INTRODUCTION REFERENCES
Novel PHEX gene locus-specific database
FGF23, hypophosphatemia, and rickets: Has phosphatonin been found? | PNAS
3 New PHEX Gene Mutations for XLH Found in Polish Children
Organization of the coding region of the PHEX/Phex gene. Exons numbered... | Download Scientific Diagram
Frontiers | Identification of a Novel Missense Mutation of the PHEX Gene in a Large Chinese Family with X-Linked Hypophosphataemia
A novel c.2179T>C mutation blocked the intracellular transport of PHEX protein and caused X‐linked hypophosphatemic rickets in a Chinese family - Li - 2020 - Molecular Genetics & Genomic Medicine - Wiley
PHEX siRNA (h), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
X-linked Hypophosphatemic Rickets | Concise Medical Knowledge
Genes | Free Full-Text | PHEXL222P Mutation Increases Phex Expression in a New ENU Mouse Model for XLH Disease
Figure 6 from Contrôle de l'expression de la protéine PHEX et rôle de PHEX et FGF23 dans la minéralisation par les cellules MC3T3 | Semantic Scholar
![PDF] Familial hypophosphatemic rickets caused by a large deletion in PHEX gene. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/722c9ab7d528737fdc210ea14aa168dd66ab33a8/4-Figure2-1.png "PDF] Familial hypophosphatemic rickets caused by a large deletion in PHEX gene. | Semantic Scholar")
PDF] Familial hypophosphatemic rickets caused by a large deletion in PHEX gene. | Semantic Scholar
Seven novel and six de novo PHEX gene mutations in patients with hypophosphatemic rickets
PHEX Gene Mutation in a Patient with X-Linked Hypophosphatemic Rickets | TACG
Mutation in Phex Gene Predisposes BALB/c-PhexHyp-Duk/Y Mice to Otitis Media | PLOS ONE
