Novel PRG4 mutations underlie CACP in Saudi families-Reference-Cited by-同舟云学术

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Novel PRG4 mutations underlie CACP in Saudi families

Published:2006-02 Issue:2 Volume:27 Page:213-213
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Alazami Anas M.,Al-Mayouf Sulaiman M.,Wyngaard Carol-Ann,Meyer Brian

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Cited by 28 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. Le syndrome de camptodactylie-arthropathie-coxa-vara-péricardite : à propos d’un cas;Revue du Rhumatisme;2024-05

2. A novel mutation in the proteoglycan 4 gene causing CACP syndrome: two sisters report;Pediatric Rheumatology;2023-01-24

3. Pseudo-rheumatic manifestations of limping: Camptodactyly–arthropathy–coxa vara–pericarditis syndrome: Single case report and review of the literature;Frontiers in Pediatrics;2022-12-05

4. Monogenic disorders as mimics of juvenile idiopathic arthritis;Pediatric Rheumatology;2022-06-18

5. Quadruped Gait and Regulation of Apoptotic Factors in Tibiofemoral Joints following Intra-Articular rhPRG4 Injection in Prg4 Null Mice;International Journal of Molecular Sciences;2022-04-12

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