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Functional characterization of mutations in inherited human cPLA(2) deficiency
Group IVA cytosolic phospholipase A(2) (cPLA(2)α) catalyzes the first step in the arachidonic acid cascade leading to the synthesis of important lipid mediators, the prostaglandins and leukotrienes. We previously described a patient deficient in cPLA(2)α activity, which was associated with mutations...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3051024/ https://ncbi.nlm.nih.gov/pubmed/21247147 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/bi101877n |
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