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Identification of two novel mutations in the SLCO2A1 prostaglandin transporter gene in a Chinese patient with primary hypertrophic osteoarthropathy
Primary hypertrophic osteoarthropathy (PHO), which is a rare multi-organic disease characterized by digital clubbing, pachydermia and periosteal reaction, typically begins during childhood or adolescence and progresses gradually over years prior to disease stabilization. To date, only two genes have...
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| Publicado no: | Mol Med Rep |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5428898/ https://ncbi.nlm.nih.gov/pubmed/28339061 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2017.6391 |
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