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1.P.263 Identification of two mutations causing familial hypercholesterolemia in Tunisia

✍ Scribed by M.N. Slimane; X.M. Sun; F. Maatoug; A.K. Soutar; M. Hammami


Book ID
119437310
Publisher
Elsevier Science
Year
1997
Tongue
English
Weight
190 KB
Volume
134
Category
Article
ISSN
0021-9150

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Familial hypercholesterolemia (FH) is a genetic disorder caused by numerous mutations in the low-density lipoprotein receptor (LDLR) gene. Mutational analyses of Indians in South Africa suggest the possibility of a high frequency of FH in India. This study aimed at identifying mutations in exons 3,