Lecithin: cholesterol acyltransferase deficiency: identification of two defective alleles in fibroblast cDNA.
Previous mutations associated with lecithin:cholesterol acyltransferase (LCAT) deficiency have been identified using genomic DNA. To facilitate mutation analysis, we used cDNA from cultured fibroblasts which were shown to express LCAT mRNA. Using reverse-transcriptase PCR, LCAT cDNA was obtained fro...
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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Elsevier
1995-05-01
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| Serie: | Journal of Lipid Research |
| Accesso online: | http://www.sciencedirect.com/science/article/pii/S0022227520398515 |
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