Clinical and biochemical characteristics of 12 Chinese primary hypertrophic osteoarthropathy patients with HPGD mutations

Primary hypertrophic osteoarthropathy (PHO) is a rare genetic disease mainly affecting the skeletal and skin. Two genes involved in prostaglandin degradation are known to be responsible for PHO: HPGD and SLCO2A1. HPGD gene mutation can cause PHO autosomal recessive 1 (PHOAR1). The purpose of the pre...

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Detalles Bibliográficos
Autores principales: Lu, Qi, Xu, Yang, Li, Shanshan, Zhang, Zeng, Sheng, Jiagen, Zhang, Zhenlin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2022
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9254467/
https://www.ncbi.nlm.nih.gov/pubmed/35813463
http://dx.doi.org/10.7150/ijbs.71261

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9254467/
https://www.ncbi.nlm.nih.gov/pubmed/35813463
http://dx.doi.org/10.7150/ijbs.71261

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