Delayed Development of Paget's Disease in Offspring InheritingSQSTM1Mutations-Reference-Cited by-同舟云学术

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Delayed Development of Paget's Disease in Offspring InheritingSQSTM1Mutations

Published:2006-12-18 Issue:3 Volume:22 Page:411-415
ISSN:0884-0431
Container-title:Journal of Bone and Mineral Research
language:en
Short-container-title:J Bone Miner Res

Author:

Bolland Mark J,Tong Pak Cheung,Naot Dorit,Callon Karen E,Wattie Diana J,Gamble Greg D,Cundy Tim

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Reference26 articles.

1. Incidence and natural history of Paget's disease of bone in England and Wales;van Staa;J Bone Miner Res,2002

2. Frequency and characteristics of familial aggregation of Paget's disease of bone;Morales-Piga;J Bone Miner Res,1995

3. Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease;Hocking;Hum Mol Genet,2002

4. Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone;Laurin;Am J Hum Genet,2002

5. Three novel mutations in SQSTM1 identified in familial Paget's disease of bone;Johnson-Pais;J Bone Miner Res,2003

Cited by 72 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. Defining the landscape of TIA1 and SQSTM1 digenic myopathy;Neuromuscular Disorders;2024-09

2. Diagnosis and treatment of Paget’s disease of bone: position paper from the Italian Society of Osteoporosis, Mineral Metabolism and Skeletal Diseases (SIOMMMS);Journal of Endocrinological Investigation;2024-03-15

3. Randomised trial of genetic testing and targeted intervention to prevent the development and progression of Paget’s disease of bone;Annals of the Rheumatic Diseases;2023-12-20

4. Update on the pathogenesis and genetics of Paget’s disease of bone;Frontiers in Cell and Developmental Biology;2022-08-12

5. Clinical phenotype of adult offspring carriers of the p.Pro392Leu mutation within the SQSTM1 gene in Paget's disease of bone;Bone Reports;2020-12

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