Molecular Diagnoses of X‐Linked and Other Genetic Hypophosphatemias: Results From a Sponsored Genetic Testing Program-Reference-Cited by-同舟云学术

Molecular Diagnoses of X‐Linked and Other Genetic Hypophosphatemias: Results From a Sponsored Genetic Testing Program

Published:2021-11-10 Issue:2 Volume:37 Page:202-214
ISSN:0884-0431
Container-title:Journal of Bone and Mineral Research
language:en
Short-container-title:J of Bone & Mineral Res

Author:

Rush Eric T.¹²³,Johnson Britt⁴,Aradhya Swaroop⁴,Beltran Daniel⁴,Bristow Sara L.⁴^ORCID,Eisenbeis Scott⁵,Guerra Norma E.⁶,Krolczyk Stan⁵,Miller Nicole⁵,Morales Ana⁴,Ramesan Prameela⁵,Sarafrazi Soodabeh⁵,Truty Rebecca⁴,Dahir Kathryn⁷

Affiliation:

1. Children's Mercy Kansas City Kansas City MO USA

2. Department of Pediatrics University of Missouri – Kansas City School of Medicine Kansas City MO USA

3. Department of Internal Medicine University of Kansas Medical Center Kansas City KS USA

4. Invitae San Francisco CA USA

5. Ultragenyx Pharmaceutical Inc. Novato CA USA

6. Department of Pediatric Nephrology Hospital General del Centro Médico Nacional «La Raza», Instituto Mexicano del Seguro Social (IMSS) Ciudad de México Mexico

7. Program for Metabolic Bone Disorders Vanderbilt University Medical Center (VUMC) Nashville TN USA

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jbmr.4454

Reference107 articles.

1. Hypophosphatemic rickets: etiology, clinical features and treatment

2. Incidence and prevalence of nutritional and hereditary rickets in southern Denmark

3. Nationwide survey of fibroblast growth factor 23 (FGF23)-related hypophosphatemic diseases in Japan: prevalence, biochemical data and treatment

4. Hereditary hypophosphatemia in Norway: a retrospective population-based study of genotypes, phenotypes, and treatment complications

5. Prevalence and Mortality of Individuals With X-Linked Hypophosphatemia: A United Kingdom Real-World Data Analysis

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