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AB008. SEPARATION and identification glycoprotein in human Fragile X syndrome serum
BACKGROUND: Fragile X syndrome (FXS), the most common cause of inherited mental retardation. The absence of FMRP results in FXS leading changes other proteins. OBJECTIVE: To detect changes of glycoproteins in human FXS serum. METHODS: Affinity chromatography with lectin concanavalin A (ConA) used to...
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| Publicado no: | Ann Transl Med |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
AME Publishing Company
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4563482/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2305-5839.2015.AB008 |
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