Correct usage of a mutated G+1 splice site and transcript quantitation in a lipoprotein lipase-deficient patient
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/2/9/1455/1724255/2-9-1455.pdf
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Pancreatitis in a Child With Lipemia Due to Novel Lipoprotein Lipase Mutations;Journal of Pediatric Gastroenterology & Nutrition;2010-04
2. Molecular pathobiology of the human lipoprotein lipase gene;Pharmacology & Therapeutics;1996-01
3. Recurrent mis-splicing of fibrillin exon 32 in two patients with neonatal Marfan syndrome;Human Molecular Genetics;1995
4. A New Italian Case of Lipoprotein Lipase Deficiency: A Leu365→Val Change Resulting in Loss of Enzyme Activity;Biochemical and Biophysical Research Communications;1994-03
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