Osteoporosis Caused by Mutations inPLS3: Clinical and Bone Tissue Characteristics-Reference-Cited by-同舟云学术

Osteoporosis Caused by Mutations inPLS3: Clinical and Bone Tissue Characteristics

Published:2014-07-21 Issue:8 Volume:29 Page:1805-1814
ISSN:0884-0431
Container-title:Journal of Bone and Mineral Research
language:en
Short-container-title:J Bone Miner Res

Author:

Fahiminiya Somayyeh¹,Majewski Jacek¹,Al-Jallad Hadil²,Moffatt Pierre²,Mort John²,Glorieux Francis H²,Roschger Paul³,Klaushofer Klaus³,Rauch Frank²

Affiliation:

1. Department of Human Genetics; Faculty of Medicine; McGill University and Genome Quebec Innovation Center; Montreal Quebec Canada

2. Shriners Hospital for Children and McGill University; Montreal Quebec Canada

3. Ludwig Boltzmann Institute of Osteology at the Hanusch Hospital of WGKK and AUVA Trauma Center Meidling; 1st Medical Department Hanusch Hospital Vienna Austria

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Reference47 articles.

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3. Idiopathic juvenile osteoporosis;Dent;Q J Med,1965

4. Osteogenesis imperfecta;Ben Amor;Pediatr Endocrinol Rev,2013

5. Relationship between genotype and skeletal phenotype in children and adolescents with osteogenesis imperfecta;Rauch;J Bone Miner Res,2010

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2. Osteoclast-specific Plastin 3 knockout in mice fail to develop osteoporosis despite dramatic increased osteoclast resorption activity;JBMR Plus;2024-01

3. PLS3 Mutations in X-Linked Osteoporosis: Clinical and Genetic Features in Five New Families;Calcified Tissue International;2023-12-03

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