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Investigation of French Canadian founder mutations for lipoprotein lipase deficiency (LPL) in France

✍ Scribed by L. Foubert; J.L. De Gennes; E. Gagne´; Y. Ma; F. Dairou; A. Raisonnier; J.P. Lagarde; M.R. Hayden; P. Benlian

Book ID
118325500
Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
158 KB
Volume
109
Category
Article
ISSN
0021-9150

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✍ France Mailly; Jutta Palmen; David P. R. Muller; Tracy Gibbs; June Lloyd; John B 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 232 KB 👁 1 views

## Communicated by Ellen Solomon The aim of this study was to identify mutations in the lipoprotein lipase (LPL) gene in 20 unrelated patients with familial lipoprotein deficiency (FLLD) and to investigate the genotype/phenotype relationship. The previously reported G188E mutation (Monsalve et al.