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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Hlavní autoři:	M Miller, K Zeller, P C Kwiterovich, J J Albers, G Feulner
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Elsevier 1995-05-01
Edice:	Journal of Lipid Research
On-line přístup:	http://www.sciencedirect.com/science/article/pii/S0022227520398515
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