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Advances in research on and diagnosis and treatment of achondroplasia in China
Achondroplasia is a rare autosomal dominant genetic disease. Research on achondroplasia in China, however, has received little emphasis. Around 80–90% of cases of neonatal achondroplasia result from mutations in fibroblast growth factor receptor 3 (FGFR3) according to polymerase chain reaction-singl...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
International Research and Cooperation Association for Bio & Socio-Sciences Advancement
2013
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4204580/ https://ncbi.nlm.nih.gov/pubmed/25343101 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2013.v2.2.45 |
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