Literature DB >> 230573

Identification of lipoprotein families in a variant of human plasma apolipoprotein A deficiency.

A Gustafson, W J McConathy, P Alaupovic, M D Curry, B Persson.   

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Year:  1979        PMID： 230573     DOI： 10.3109/00365517909106122

Source DB:  PubMed          Journal:  Scand J Clin Lab Invest        ISSN： 0036-5513            Impact factor:   1.713


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  5 in total

1.  High density lipoprotein deficiency with xanthomas. A defect in reverse cholesterol transport caused by a point mutation in the apolipoprotein A-I gene.

Authors:  K J Lackner; H Dieplinger; G Nowicka; G Schmitz
Journal:  J Clin Invest       Date:  1993-11       Impact factor: 14.808

2.  A frameshift mutation in the human apolipoprotein A-I gene causes high density lipoprotein deficiency, partial lecithin: cholesterol-acyltransferase deficiency, and corneal opacities.

Authors:  H Funke; A von Eckardstein; P H Pritchard; M Karas; J J Albers; G Assmann
Journal:  J Clin Invest       Date:  1991-01       Impact factor: 14.808

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

Authors:  T Matsunaga; Y Hiasa; H Yanagi; T Maeda; N Hattori; K Yamakawa; Y Yamanouchi; I Tanaka; T Obara; H Hamaguchi
Journal:  Proc Natl Acad Sci U S A       Date:  1991-04-01       Impact factor: 11.205

4.  Apolipoprotein A-I Q[-2]X causing isolated apolipoprotein A-I deficiency in a family with analphalipoproteinemia.

Authors:  D S Ng; L A Leiter; C Vezina; P W Connelly; R A Hegele
Journal:  J Clin Invest       Date:  1994-01       Impact factor: 14.808

5.  Clinical and histopathological features of a suspected case of fish-eye disease.

Authors:  Hiroko Tateno; Makoto Taomoto; Nobuo Jo; Kanji Takahashi; Yoshiko Uemura
Journal:  Jpn J Ophthalmol       Date:  2012-08-02       Impact factor: 2.447
  5 in total

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