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Limited mutational heterogeneity in the LDLR gene in familial hypercholesterolemia in Tunisia

✍ Scribed by A. Jelassi; I. Jguirim; M. Najah; A.M. Abid; L. Boughamoura; F. Maatouk; M. Rouis; C. Boileau; J.P. Rabès; M.N. Slimane; M. Varret


Book ID
118422213
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
225 KB
Volume
203
Category
Article
ISSN
0021-9150

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✍ Luis A. Salazar; Mario H. Hirata; Selma A. Cavalli; Edna R. Nakandakare; Neusa F 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 150 KB 👁 1 views

## Communicated by Mark H. Paalman Low-density lipoprotein receptor (LDLR) gene mutations cause familial hypercholesterolemia (FH), one of the most common single gene disorders. The spectrum of LDLR mutations in Brazil is not known. The aim of this study was the characterization of LDLR mutations