Mutations in theSLCO2A1Gene and Primary Hypertrophic Osteoarthropathy: A Clinical and Biochemical Characterization-Reference-Cited by-同舟云学术

Mutations in theSLCO2A1Gene and Primary Hypertrophic Osteoarthropathy: A Clinical and Biochemical Characterization

Published:2013-05-01 Issue:5 Volume:98 Page:E923-E933
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:

Author:

Zhang Zeng¹²,He Jin-Wei¹,Fu Wen-Zhen¹,Zhang Chang-Qing²,Zhang Zhen-Lin¹

Affiliation:

1. Metabolic Bone Disease and Genetic Research Unit (Z.Z., J.-W.H., W.-Z.F., Z.-L.Z.), Shanghai 200233, People's Republic of China

2. Department of Osteoporosis and Bone Diseases, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, and Department of Orthopedic Surgery (Z.Z., C.-Q.Z.), Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai 200233, People's Republic of China

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/98/5/E923/9049298/jcemE923.pdf

Reference40 articles.

1. Mendelian disorders deserve more attention;Antonarakis;Nat Rev Genet,2006

2. The clinical spectrum of pachydermoperiostosis (primary hypertrophic osteoarthropathy);Matucci-Cerinic;Medicine (Baltimore),1991

3. Pachydermoperiostosis (idiopathic clubbing and periostosis): genetic and physiologic considerations;Rimoin;N Engl J Med,1965

4. Pachydermoperiostosis: an update;Castori;Clin Genet,2005

5. Primary hypertrophic osteoarthropathy;Martinez-Lavin;Semin Arthritis Rheum,1988

Cited by 58 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. Pachydermoperiostosis Presenting With End-Stage Kidney Disease;Cureus;2024-06-14

2. Clinical and genetic characteristics of Chinese patients diagnosed with chronic enteropathy associated with SLCO2A1 gene;Orphanet Journal of Rare Diseases;2024-05-16

3. HYPERTROPHIC OSTEOARTHROPATHY IN A PATIENT WITH HETEROZYGOUS MUTATION IN THE SLCO2A1 GENE: A CASE REPORT;Central Asian Journal of Medical Hypotheses and Ethics;2023-12-29

4. Features of the clinical course of pachydermoperiostosis with a verified mutation in the European type gene;Osteoporosis and Bone Diseases;2023-11-15

5. Primary hypertrophic osteoarthropathy: genetics, clinical features and management;Frontiers in Endocrinology;2023-08-29