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New therapeutic targets in rare genetic skeletal diseases
Introduction: Genetic skeletal diseases (GSDs) are a diverse and complex group of rare genetic conditions that affect the development and homeostasis of the skeleton. Although individually rare, as a group of related diseases, GSDs have an overall prevalence of at least 1 per 4,000 children. There a...
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| Publicat a: | Expert Opin Orphan Drugs |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Informa Healthcare
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4643203/ https://ncbi.nlm.nih.gov/pubmed/26635999 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1517/21678707.2015.1083853 |
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