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A novel PHEX mutation associated with vitamin D-resistant rickets | Human Genome Variation
PHEX Gene - GeneCards | PHEX Protein | PHEX Antibody
Seven novel and six de novo PHEX gene mutations in patients with hypophosphatemic rickets
CASE REPORT MOLECULAR ANALYSIS CONCLUSION INTRODUCTION REFERENCES
Diagram of the PHEX gene showing the mutations detected in this study... | Download Scientific Diagram
Whole Exome Sequencing Reveals Novel PHEX Splice Site Mutations in Patients with Hypophosphatemic Rickets | PLOS ONE
FGF23 and its role in X-linked hypophosphatemia-related morbidity | Orphanet Journal of Rare Diseases | Full Text
Genes | Free Full-Text | Impact of X-Linked Hypophosphatemia on Muscle Symptoms
Frontiers | Clinical and Genetic Characteristics of 153 Chinese Patients With X-Linked Hypophosphatemia
JCI - Aberrant Phex function in osteoblasts and osteocytes alone underlies murine X-linked hypophosphatemia
PHEX Gene Mutations and Genotype-Phenotype Analysis of Korean Patients with Hypophosphatemic Rickets
Novel PHEX gene locus-specific database
Mutation in Phex Gene Predisposes BALB/c-PhexHyp-Duk/Y Mice to Otitis Media | PLOS ONE
Organization of the coding region of the PHEX/Phex gene. Exons numbered... | Download Scientific Diagram
Phenotypes of a family with XLH with a novel PHEX mutation | Human Genome Variation
Seven novel and six de novo PHEX gene mutations in patients with hypophosphatemic rickets
FGF23, PHEX, and MEPE regulation of phosphate homeostasis and skeletal mineralization | American Journal of Physiology-Endocrinology and Metabolism
![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
PHEX gene mutation in a Chinese family with six cases of X-linked hypophosphatemic rickets
Genotype–phenotype analysis, and assessment of the importance of the zinc-binding site in PHEX in Japanese patients with X-linked hypophosphatemic rickets using 3D structure modeling - ScienceDirect
Genetic Testing Confirmed the Early Diagnosis of X-Linked Hypophosphatemic Rickets in a 7-Month-Old Infant - Kok Siong Poon, Andrew Anjian Sng, Cindy Weili Ho, Evelyn Siew-Chuan Koay, Kah Yin Loke, 2015
PHEX gene and hypophosphatemia - ScienceDirect
Genes | Free Full-Text | PHEXL222P Mutation Increases Phex Expression in a New ENU Mouse Model for XLH Disease
