Assessment of French patients with LPL deficiency for French Canadian mutations.

Author:

Foubert L,De Gennes J L,Lagarde J P,Ehrenborg E,Raisonnier A,Girardet J P,Hayden M R,Benlian P

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference37 articles.

1. Human lipoprotein lipase complementary DNA sequence;Wion, K.; Kirchgessner, T.; Lusis, A.J.; Schotz, M.C.; Lawn, R.M.;Science,1987

2. Genetic variants affecting human lipoprotein and hepatic lipases;Hayden, M.R.; Ma, Y.; Brunzell, J.; Henderson, H.E.;Curr Opin Lipidol,1991

3. La lipoproteine lipase, enzyme du remodelage des lipoproteines riches en triglycerides. In: Genetique et dyslipidimies;Benlian, P.,1996

4. Amino acid substitution (Ile"'4Thr) in exon 5 of the lipoprotein lipase gene causes lipoprotein lipase deficiency in three unrelated probands. Support for multicentric origin;Henderson, H.E.; Ma, Y.; Hassan, M.F.;Jf Clin Invest,1991

5. Recurrent missense mutations at the first and second base of codon ARG243 in human lipoprotein lipase causing chylomicronemia in patients of different ancestries;Ma, Y.; Liu, M.S.; Chitayat, D.;Hum Mutat,1994

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