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Apolipoprotein A-I deficiency due to a codon 84 nonsense mutation of the apolipoprotein A-I gene.

The molecular genetic defect of a female patient with apolipoprotein A-I (apoA-I) deficiency and premature atherosclerosis was examined. Her parents were first cousins. Her plasma density fraction from 1.063 to 1.21 g/ml contained no apoA-I on SDS/PAGE and no measurable high density lipoprotein chol...

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Hlavní autoři: Matsunaga, T, Hiasa, Y, Yanagi, H, Maeda, T, Hattori, N, Yamakawa, K, Yamanouchi, Y, Tanaka, I, Obara, T, Hamaguchi, H
Médium: Artigo
Jazyk:Inglês
Vydáno: 1991
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC51325/
https://ncbi.nlm.nih.gov/pubmed/1901417
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