Juvenile Paget’s disease with compound heterozygous mutations in TNFRSF11B presenting with recurrent clavicular fractures and a mild skeletal phenotype-Reference-Cited by-同舟云学术

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Juvenile Paget’s disease with compound heterozygous mutations in TNFRSF11B presenting with recurrent clavicular fractures and a mild skeletal phenotype

Published:2020-01 Issue: Volume:130 Page:115098
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Naot Dorit,Wilson Louise C.,Allgrove Jeremy,Adviento Eleanor,Piec Isabelle,Musson David S.,Cundy Tim,Calder Alistair D.

Funder

Health Research Council of New Zealand

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference25 articles.

1. Fragile bones and macrocranium;Bakwin;J. Pediatr.,1956

2. Juvenile paget disease;Polyzos;Metabolism,2018

3. Idiopathic hyperphosphatasia and TNFRSF11B mutations: relationships between phenotype and genotype;Chong;J. Bone Miner. Res.,2003

4. Auricular ossification: a newly recognized feature of osteoprotegerin-deficiency juvenile Paget disease;Gottesman;Am. J. Med. Genet. A,2016

5. Ocular manifestations of juvenile Paget disease;Kerr;Arch. Ophthalmol.,2010

Cited by 3 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. A hybrid systems biology and systems pharmacology investigation of Zingerone’s effects on reconstructed human epidermal tissues;Egyptian Journal of Medical Human Genetics;2021-12

2. Genetic disorders associated with the RANKL/OPG/RANK pathway;Journal of Bone and Mineral Metabolism;2020-09-17

3. Juvenile Paget's Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor SP7);Bone;2020-08

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