Identification of mutations in the prostaglandin transporter gene SLCO2A1 and phenotypic comparison between two subtypes of primary hypertrophic osteoarthropathy (PHO): A single-center study-Reference-Cited by-同舟云学术

Identification of mutations in the prostaglandin transporter gene SLCO2A1 and phenotypic comparison between two subtypes of primary hypertrophic osteoarthropathy (PHO): A single-center study

Published:2018-01 Issue: Volume:106 Page:96-102
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Hou Yanfang,Lin Yuanyuan,Qi Xuan,Yuan Lu,Liao Ruoxi,Pang Qianqian,Cui Lijia,Jiang Yan,Wang Ou,Li Mei,Dong Jin,Xia Weibo

Funder

National Natural Science Foundation of China

National Science and Technology Pillar Program

National Science and Technology Major Projects for “Major New Drugs Innovation and Development”

Beijing Natural Science Foundation

National Key Program of Clinical Science

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference24 articles.

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4. Mutations in 15-hydroxyprostaglandin dehydrogenase cause primary hypertrophic osteoarthropathy;Uppal;Nat. Genet.,2008

5. Exome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathy;Zhang;Am. J. Hum. Genet.,2012

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