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Schematic representation of the PHEX gene with the localization of the... |  Download Scientific Diagram
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
Organization of the coding region of the PHEX/Phex gene. Exons numbered... | Download Scientific Diagram

XLH Overview | For HCPs
XLH Overview | For HCPs

Seven novel and six de novo PHEX gene mutations in patients with  hypophosphatemic rickets
Seven novel and six de novo PHEX gene mutations in patients with hypophosphatemic rickets

Novel PHEX gene locus-specific database
Novel PHEX gene locus-specific database

PHEX Gene - GeneCards | PHEX Protein | PHEX Antibody
PHEX Gene - GeneCards | PHEX Protein | PHEX Antibody

Figure 2 from A Novel PHEX Gene Mutation in a Patient with Sporadic  Hypophosphatemic Rickets | Semantic Scholar
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
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
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
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
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
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 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
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
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
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
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
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 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 siRNA (h), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology

PHEX Gene - GeneCards | PHEX Protein | PHEX Antibody
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
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
JCI - Aberrant Phex function in osteoblasts and osteocytes alone underlies murine X-linked hypophosphatemia

Novel PHEX gene locus-specific database
Novel PHEX gene locus-specific database

FGF23, hypophosphatemia, and rickets: has phosphatonin been found? -  Abstract - Europe PMC
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
Whole Exome Sequencing Reveals Novel PHEX Splice Site Mutations in Patients with Hypophosphatemic Rickets | PLOS ONE