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Prevalence of Lithuanian mutation among St. Petersburg Jews with familial hypercholesterolemia

✍ Scribed by Mikhail Mandelshtam; Khalid Chakir; Sergei Shevtsov; Valery Golubkov; Natalya Skobeleva; Boris Lipovetsky; Vladimir Konstantinov; Alexander Denisenko; Vladimir Gaitskhoki; Eugene Schwartz


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
184 KB
Volume
12
Category
Article
ISSN
1059-7794

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✦ Synopsis


We used polymerase chain reaction-single-strand conformation polymorphism (PCR-SSCP) analysis to detect LDL receptor gene defects in the St. Petersburg population. We have found a deltaG197 mutation in several patients of Jewish origin. The mutation named is shown to be responsible for onethird (7/23) of familial hypercholesterolemia (FH) cases in St. Petersburg Jews and absent in patients of Russian descent. The prevalence of a deltaG197 mutation in St. Petersburg Jews is consistent with its origin in Lithuania or Poland. The deltaG197 mutation can be easily detected in polyacrylamide minigels because of formation of specific heteroduplexes during PCR with DNA of heterozygous patients. Taken together with high prevalence of the mutation in St. Petersburg Jews, this observation provides an opportunity for DNA diagnostics of FH in this ethnic group.