Clinical and genetic analysis in a large Chinese cohort of patients with X-linked hypophosphatemia-Reference-Cited by-同舟云学术

Clinical and genetic analysis in a large Chinese cohort of patients with X-linked hypophosphatemia

Published:2019-04 Issue: Volume:121 Page:212-220
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Zhang Cong,Zhao Zhen,Sun Yue,Xu Lijun,JiaJue Ruizhi,Cui Lijia,Pang Qianqian,Jiang Yan,Li Mei,Wang Ou,He Xiaodong,He Shuli,Nie Min,Xing Xiaoping,Meng Xunwu,Zhou Xueying,Yan Lina,Kaplan Jared M.,Insogna Karl L.,Xia Weibo

Funder

National Science and Technology Major Projects for New Drugs Innovation and Development

National Natural Science Foundation of China

National Key Program of Clinical Science

Beijing Natural Science Foundation

CAMS Innovation Fund for Medical Sciences

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference47 articles.

1. Incidence and prevalence of nutritional and hereditary rickets in southern Denmark;Beck-Nielsen;Eur. J. Endocrinol.,2009

2. A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets;Francis;Nat. Genet.,1995

3. FGF23 production by osteocytes;Bonewald;Pediatr. Nephrol.,2013

4. Increased circulatory level of biologically active full-length FGF-23 in patients with hypophosphatemic rickets/osteomalacia;Yamazaki;J. Clin. Endocrinol. Metab.,2002

5. FGF-23 is a potent regulator of vitamin D metabolism and phosphate homeostasis;Shimada;J. Bone Miner. Res.,2004

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