X-linked hypophosphatemia caused by a deep intronic variant in PHEX identified by PCR-based RNA analysis of urine-derived cells-Reference-Cited by-同舟云学术

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X-linked hypophosphatemia caused by a deep intronic variant in PHEX identified by PCR-based RNA analysis of urine-derived cells

Published:2023-11 Issue: Volume:176 Page:116839
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Grimbly Chelsey,Ludwig Karissa,Wu Zenghui,Caluseriu Oana,Rosolowsky Elizabeth,Alexander R. Todd,Ward Leanne M.,Rauch Frank

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference25 articles.

1. Skeletal and extraskeletal disorders of biomineralization;Collins;Nat. Rev. Endocrinol.,2022

2. Mineralized tissues in hypophosphatemic rickets;Robinson;Pediatr. Nephrol.,2020

3. Osteopontin and the dento-osseous pathobiology of X-linked hypophosphatemia;Boukpessi;Bone.,2017

4. Alterations of bone material properties in adult patients with X-linked hypophosphatemia (XLH);Fratzl-Zelman;J. Struct. Biol.,2020

5. Molecular diagnoses of X-linked and other genetic hypophosphatemias: results from a sponsored genetic testing program;Rush;J. Bone Miner. Res.,2022

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Familial cases with adult-onset FGF23-related hypophosphatemic osteomalacia -A PHEX 3’-UTR change as a possible cause-;Bone;2024-05

2. Recent advances in fibroblast growth factor 23-related hypophosphatemic disorders;Current Opinion in Endocrinology, Diabetes & Obesity;2024-05-01

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