Schematic representation of the PHEX gene with the localization of the... | Download Scientific Diagram
Organization of the coding region of the PHEX/Phex gene. Exons numbered... | Download Scientific Diagram
XLH Overview | For HCPs
Seven novel and six de novo PHEX gene mutations in patients with hypophosphatemic rickets
Novel PHEX gene locus-specific database
PHEX Gene - GeneCards | PHEX Protein | PHEX Antibody
Figure 2 from A Novel PHEX Gene Mutation in a Patient with Sporadic Hypophosphatemic Rickets | Semantic Scholar
FGF23 and its role in X-linked hypophosphatemia-related morbidity | Orphanet Journal of Rare Diseases | Full Text
Seven novel and six de novo PHEX gene mutations in patients with hypophosphatemic rickets
Frontiers | Clinical and Genetic Characteristics of 153 Chinese Patients With X-Linked Hypophosphatemia
Phosphorus metabolism in XLH. Inactivation of PHEX gene results in... | Download Scientific Diagram
Mutation in Phex Gene Predisposes BALB/c-PhexHyp-Duk/Y Mice to Otitis Media | PLOS ONE
FGF23 and its role in X-linked hypophosphatemia-related morbidity | Orphanet Journal of Rare Diseases | Full Text
FGF23, PHEX, and MEPE regulation of phosphate homeostasis and skeletal mineralization | American Journal of Physiology-Endocrinology and Metabolism
PHEX gene mutation in a Chinese family with six cases of X-linked hypophosphatemic rickets
Genes | Free Full-Text | PHEXL222P Mutation Increases Phex Expression in a New ENU Mouse Model for XLH Disease
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 Mutations and Genotype-Phenotype Analysis of Korean Patients with Hypophosphatemic Rickets
PHEX siRNA (h), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
PHEX Gene - GeneCards | PHEX Protein | PHEX Antibody
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Functional Characterization of PHEX Gene Variants in Children With X‐Linked Hypophosphatemic Rickets Shows No Evidence of Genotype–Phenotype Correlation - Zheng - 2020 - Journal of Bone and Mineral Research - Wiley Online Library
JCI - Aberrant Phex function in osteoblasts and osteocytes alone underlies murine X-linked hypophosphatemia
Novel PHEX gene locus-specific database
FGF23, hypophosphatemia, and rickets: has phosphatonin been found? - Abstract - Europe PMC
Whole Exome Sequencing Reveals Novel PHEX Splice Site Mutations in Patients with Hypophosphatemic Rickets | PLOS ONE