Identification of mutations in the prostaglandin transporter gene SLCO2A1 and its phenotype–genotype correlation in Japanese patients with pachydermoperiostosis-Reference-Cited by-同舟云学术

Identification of mutations in the prostaglandin transporter gene SLCO2A1 and its phenotype–genotype correlation in Japanese patients with pachydermoperiostosis

Published:2012-10 Issue:1 Volume:68 Page:36-44
ISSN:0923-1811
Container-title:Journal of Dermatological Science
language:en
Short-container-title:Journal of Dermatological Science

Author:

Sasaki Takashi,Niizeki Hironori,Shimizu Atsushi,Shiohama Aiko,Hirakiyama Asami,Okuyama Torayuki,Seki Atsuhito,Kabashima Kenji,Otsuka Atsushi,Ishiko Akira,Tanese Keiji,Miyakawa Shun-ichi,Sakabe Jun-ichi,Kuwahara Masamitsu,Amagai Masayuki,Okano Hideyuki,Suematsu Makoto,Kudoh Jun

Publisher

Elsevier BV

Subject

Dermatology,Molecular Biology,Biochemistry

Reference24 articles.

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

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

3. Un syndrome ostéodermopathique: la pachydermieplicaturée avec pachypé riostose des extrémités;Touraine;Presse Med,1935

4. Primary hypertrophic osteoarthropathy with digital clubbing and palmoplantar hyperhidrosis caused by 15-PGHD/HPGD loss-of-function mutations;Bergmann;Exp Dermatol,2011

5. Common and recurrent HPGD mutations in Caucasian individuals with primary hypertrophic osteoarthropathy;Diggle;Rheumatology (Oxford),2010

Cited by 68 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. Lack of cutis verticis gyrata is associated with c.1279_1290del12 of SLCO2A1 in 43 Japanese patients with pachydermoperiostosis;Journal of Dermatological Science;2024-05

2. Complete pachydermoperiostosis: A case report;Electronic Journal of General Medicine;2024-01-01

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

4. Reclassification of theHPGDp.Ala13Glu variant causing primary hypertrophic osteoarthropathy;Molecular Case Studies;2023-08-17

5. A novel compound mutation of SLCO2A1 in a Chinese patient with Primary hypertrophic osteoarthropathy;Indian Journal of Dermatology, Venereology and Leprology;2023-07-27