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Phenotypic effects of Ehlers–Danlos syndrome-associated mutation on the FnIII domain of tenascin-X
Tenascin-X (TNX) is an extracellular matrix (ECM) protein and interacts with a wide variety of molecules in the ECM as well as on the membrane. Deficiency of TNX causes a recessive form of Ehlers–Danlos syndrome (EDS) characterized by hyperelastic and fragile skin, easy bruising, and hypermobile joi...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wiley Subscription Services, Inc., A Wiley Company
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3005793/ https://ncbi.nlm.nih.gov/pubmed/20853426 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/pro.503 |
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